Doctor Jobs in Chennai

Why This Role MattersThe Dental Surgeon role is essential for delivering quality oral healthcare services to patients. Dental surgeons diagnose and treat dental conditions such as tooth decay, gum disease, and oral infections while also performing preventive and restorative dental procedures. By providing timely treatment and maintaining accurate patient records, this role helps improve patients’ oral health and supports the efficient functioning of the dental clinic.Job DescriptionSmile and Shine Dental Clinic is hiring a Dental Surgeon for a full-time or part-time position in Chennai, Tamil Nadu. The role involves diagnosing dental conditions, providing routine and advanced dental treatments, and maintaining patient records. The selected candidate will work closely with patients to ensure high standards of dental care and treatment outcomes.Key Features of the Role• Position: Dental Surgeon• Company: Smile and Shine Dental Clinic• Location: Chennai, Tamil Nadu, India• Employment Type: Full-Time / Part-Time• Workplace Type: On-site• Salary: ₹10,000 – ₹15,000 per month (may vary based on experience)• Experience Required: Minimum 1 yearResponsibilities• Diagnose and treat dental conditions such as tooth decay, gum disease, and infections• Perform routine dental examinations and preventive treatments• Provide dental procedures including fillings, extractions, and basic restorative treatments• Conduct patient assessments and prepare treatment plans• Maintain accurate medical records and dental documentation• Educate patients about oral hygiene and preventive dental care• Ensure proper sterilization and hygiene protocols in the clinic• Coordinate with clinic staff to maintain smooth daily operationsRequired Qualification• Bachelor of Dental Surgery (BDS) from a recognized institutionImportant Requirements• Minimum 1 year of experience in a dental clinic (preferred)• Ability to commute to or relocate to Chennai before starting work• Good patient assessment and communication skills• Knowledge of medical terminology and dental documentationEmployment Options• Full-time dental surgeon position• Part-time opportunity availableWhat We Offer• Opportunity to work in a clinical dental practice• Exposure to a variety of dental procedures and patient cases• Supportive clinic environment• Flexible employment options (full-time or part-time)Experience and Skills• Patient assessment and diagnosis• General dentistry procedures• Medical records and clinical documentation• Knowledge of dental terminology• Communication and patient managementSalary Insights• Salary: ₹10,000 – ₹15,000 per month• Salary may vary depending on experience and responsibilitiesCompany OverviewSmile and Shine Dental Clinic is a dental healthcare provider based in Chennai, offering general dental treatments and preventive oral care services. The clinic focuses on delivering quality patient care through professional dental treatment and maintaining a supportive clinical environment.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) degree.How much experience is required?A minimum of 1 year of experience as a dentist is preferred.What is the salary for this role?The salary ranges from ₹10,000 to ₹15,000 per month depending on experience.Is this a full-time position?Both full-time and part-time positions are available.Application Tips• Highlight clinical experience in general dentistry procedures• Mention experience in patient assessment and dental documentation• Emphasize communication and patient handling skills• Include experience performing common dental procedures

Why This Role MattersThe General Dental Surgeon plays a key role in providing quality dental care and maintaining patients’ oral health. This role involves diagnosing dental conditions, performing routine procedures, and ensuring patients receive safe, comfortable, and effective treatment. At Radiant Dental Care, the position contributes to delivering reliable and patient-focused dental services in a modern clinical setting.Job DescriptionRadiant Dental Care is hiring a passionate and skilled General Dental Surgeon to join its dental team in Sholinganallur, Chennai. The ideal candidate should be confident in diagnosing dental problems and performing routine dental procedures while maintaining high standards of patient care. Fresh graduates who are enthusiastic about building their clinical experience are encouraged to apply.Key Features of the Role• Opportunity to work in a professional dental clinic environment• Exposure to routine dental diagnosis and treatment procedures• Patient-focused clinical practice• Suitable opportunity for fresh dental graduates starting their careersResponsibilities• Diagnose dental conditions and recommend appropriate treatment plans• Perform routine dental procedures such as fillings, extractions, and scaling• Provide preventive dental care and oral health education to patients• Maintain accurate patient records and treatment documentation• Ensure infection control and sterilization protocols are followed• Deliver high standards of patient care and ensure patient comfort during procedures• Collaborate with dental staff for smooth clinic operationsRequired Qualification• Bachelor of Dental Surgery (BDS)Important Requirements• Valid dental qualification from a recognized institution• Good clinical knowledge of general dentistry• Strong patient care approach and communication skills• Ability to diagnose and perform routine dental proceduresEmployment Options• Full-time position• Fresher candidates are welcome to applyWhat We Offer• Opportunity to gain clinical experience in a professional dental setup• Supportive and collaborative working environment• Exposure to a variety of routine dental treatments• Career growth opportunities in dentistryExperience and Skills• Freshers or entry-level dentists can apply• Basic clinical skills in general dentistry• Strong communication and patient management skills• Attention to detail and commitment to quality careSalary InsightsThe salary for this position ranges from ₹25,000 to ₹40,000 per month, depending on qualifications, clinical skills, and experience.Company OverviewRadiant Dental Care is a dental clinic located in Sholinganallur, Chennai, offering comprehensive dental services and focusing on high-quality patient care. The clinic is dedicated to maintaining professional standards in dentistry while providing a comfortable environment for patients.FAQs1. Who can apply for this role?Candidates with a Bachelor of Dental Surgery (BDS) degree can apply. Freshers are welcome.2. Is prior experience required?No. This position is open to fresh graduates starting their dental careers.3. What is the work location?The job is based in Sholinganallur, Chennai, Tamil Nadu.4. What is the salary range?The salary ranges from ₹25,000 to ₹40,000 per month.Application Tips• Highlight your BDS qualification and internship experience in your resume.• Mention any clinical procedures you have assisted with or performed during training.• Emphasize patient communication skills and attention to detail.• Prepare to discuss basic dental diagnosis and treatment procedures during the interview.

Why This Role MattersThe Resident Dentist role at Sinora Dental Clinic plays an important role in delivering quality dental care and supporting patients in maintaining good oral health. This position helps the clinic provide professional diagnosis, routine dental procedures, and preventive care while ensuring patients receive comfortable and reliable treatment.Job DescriptionSinora Dental Clinic is hiring a Resident Dentist for its new multi-speciality dental clinic in Ashok Nagar, Chennai. The clinic is looking for a sincere and committed dental graduate who is passionate about dentistry and patient care. Freshers are welcome to apply, and the clinic offers a friendly working environment along with exposure to modern dental technology.Key Features of the Role• Position: Resident Dentist• Organization: Sinora Dental Clinic• Location: Chennai, Tamil Nadu, India• Employment Type: Full-time / Part-time / Permanent• Salary Range: ₹25,000 per month• Experience Level: Freshers and experienced candidatesResponsibilities• Diagnose dental conditions and assess patients’ oral health• Perform routine dental procedures and treatments• Provide consultations and treatment planning for patients• Educate patients about oral hygiene and preventive dental care• Maintain accurate patient records and treatment documentation• Follow clinic protocols for sterilization and infection control• Ensure patient comfort and high-quality dental careRequired Qualification• Bachelor of Dental Surgery (BDS)Important Requirements• Strong commitment and sincerity towards clinical work• Good communication and interpersonal skills• Ability to perform general dental procedures• Willingness to learn and work with modern dental technology• Professional attitude toward patient careWhat We Offer• Opportunity to work in a multi-speciality dental clinic• Friendly and supportive work environment• Exposure to modern dental technology and procedures• Hands-on clinical experience for fresh graduatesExperience and Skills• Dental diagnosis and treatment procedures• Patient consultation and communication• Preventive dental care and oral hygiene guidance• Clinical documentation and patient record management• Infection control and sterilization practicesSalary Insights• ₹25,000 per monthCompany OverviewSinora Dental Clinic is a multi-speciality dental clinic located in Ashok Nagar, Chennai. The clinic focuses on providing comprehensive dental care using modern technology and maintaining a patient-friendly environment. It aims to deliver quality dental treatments while supporting dental professionals in gaining valuable clinical experience.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) degree.Where is the job located?The position is based in Chennai, Tamil Nadu, India.What salary is offered for this role?The salary offered is ₹25,000 per month.Are freshers eligible for this role?Yes, fresh dental graduates are welcome to apply.What type of employment is offered?The clinic offers full-time, part-time, and permanent employment options.Application Tips• Highlight your BDS qualification and internship experience• Mention dental procedures you are confident performing• Demonstrate strong communication and patient handling skills• Show willingness to learn modern dental technologies• Maintain a professional and patient-focused attitude during interviews

Why This Role MattersPharmacovigilance is a critical function in the pharmaceutical and healthcare industry that focuses on monitoring, detecting, assessing, and preventing adverse drug reactions. Ensuring the safety of medicines after they reach the market is essential for protecting patients and maintaining trust in healthcare systems. Professionals working in pharmacovigilance contribute to global drug safety by identifying potential risks associated with medicines and ensuring that these risks are reported and managed according to international regulatory standards.In this role, the Pharmacovigilance Services Associate supports drug safety surveillance activities by managing safety case reports, reviewing adverse event information, and ensuring accurate documentation in global safety databases. The role also involves collaboration with regulatory teams and healthcare stakeholders to ensure compliance with pharmacovigilance guidelines. Working with a global professional services organization like Accenture provides exposure to international pharmacovigilance processes and opportunities to contribute to large-scale healthcare and pharmaceutical safety programs.Job DescriptionAccenture is hiring Pharmacovigilance Services Associates to support its Pharmacovigilance Operations and Drug Safety Surveillance team. This position focuses on identifying, reviewing, and processing adverse event reports in compliance with global pharmacovigilance regulations and client-specific standard operating procedures.The role requires professionals to manage Individual Case Safety Reports (ICSRs), monitor safety information received from multiple sources, and ensure accurate data entry and processing in global safety databases. The associate will also assist in evaluating adverse drug reactions, performing medical coding, and ensuring that safety reports are submitted within regulatory timelines.Candidates will work with cross-functional teams including regulatory affairs specialists, safety scientists, and pharmacovigilance experts. This role offers an excellent opportunity for life sciences graduates who want to build a long-term career in pharmacovigilance, drug safety, regulatory affairs, and pharmaceutical risk management.Key Features of the Role• Job Title: Pharmacovigilance Services Associate / Drug Safety Associate• Department: Pharmacovigilance Operations – Drug Safety Surveillance• Organization: Accenture• Experience Required: 1–3 years• Qualification: BAMS / Bachelor’s or Master’s Degree in Life Sciences• Industry: Pharmaceutical Safety & Healthcare Services• Work Environment: Global pharmacovigilance operations teamResponsibilitiesCase Intake and Case Creation• Identify and create safety cases in the global safety database from reports received via intake workflows, client mailboxes, electronic gateways, and other reporting sources.• Retrieve new incoming safety information and follow-up correspondence for existing safety cases.• Ensure that all safety cases are recorded accurately and processed according to client guidelines and regulatory requirements.Adverse Event Monitoring and Evaluation• Collect, evaluate, and document Adverse Events (AE), Serious Adverse Events (SAE), and Suspected Unexpected Serious Adverse Reactions (SUSAR).• Verify the validity of Individual Case Safety Reports and ensure that cases meet regulatory reporting criteria.• Perform duplicate checks and review case data to confirm medical significance and accuracy.Case Processing and Data Management• Conduct case triage, prioritization, and data entry for safety cases in the pharmacovigilance database.• Process ICSRs end-to-end according to regulatory deadlines, service-level agreements, and internal quality standards.• Ensure all safety case information is complete, accurate, and consistent across systems.Medical Coding and Documentation• Perform medical coding using internationally recognized dictionaries such as MedDRA and WHO Drug Dictionary.• Document clinical information, patient history, suspect drug information, and adverse reactions.• Prepare detailed safety narratives and maintain proper pharmacovigilance documentation.Regulatory Reporting and Compliance• Submit adverse event reports to global safety databases and regulatory authorities when required.• Monitor report submissions and troubleshoot issues related to safety data transmission.• Ensure that pharmacovigilance activities comply with international regulatory guidelines and company SOPs.Quality Assurance and Follow-Up• Review safety case data for completeness, accuracy, and regulatory compliance.• Identify missing information and request clarification from reporters or marketing companies when necessary.• Track follow-up actions and ensure resolution of pending safety case items.Operational Support and Collaboration• Work closely with pharmacovigilance teams, regulatory partners, and cross-functional departments.• Support pharmacovigilance audits, inspections, and compliance activities.• Assist in preparing pharmacovigilance meeting minutes, documentation, and safety report tracking.Required Qualifications• Bachelor’s Degree in Life Sciences or related discipline.• Bachelor of Ayurvedic Medicine and Surgery (BAMS) or Master’s Degree in Life Sciences.• Basic understanding of pharmacovigilance processes, adverse event reporting, and drug safety monitoring.Educational RequirementsCandidates must hold one of the following qualifications from a recognized institution:• Bachelor’s Degree in Life Sciences• Master’s Degree in Life Sciences• Bachelor of Ayurvedic Medicine and Surgery (BAMS)These academic backgrounds provide the scientific foundation needed to understand drug safety concepts, medical terminology, and pharmacovigilance workflows.Experience and SkillsExperience• 1–3 years of experience in pharmacovigilance operations or drug safety surveillance.• Experience in handling Individual Case Safety Reports and safety database systems is preferred.Technical Skills• Knowledge of pharmacovigilance safety databases and case processing workflows.• Familiarity with medical coding dictionaries such as MedDRA and WHO-Drug.• Proficiency in Microsoft Office tools for documentation and reporting.Professional Skills• Strong medical writing and documentation abilities.• Excellent English communication skills including reading, writing, listening, and speaking.• Ability to work efficiently in a fast-paced environment while maintaining accuracy.• Strong analytical thinking and attention to detail.• Commitment to regulatory compliance and quality standards.Salary InsightsPharmacovigilance professionals in India typically receive competitive salary packages depending on experience and technical expertise. Associates with one to three years of experience can expect industry-standard compensation along with opportunities for career development, training programs, and exposure to global pharmacovigilance operations.Company OverviewAccenture is a global professional services company known for its expertise in consulting, technology services, digital transformation, and business operations. With a presence in more than 120 countries, the organization supports clients across industries including healthcare, pharmaceuticals, finance, and technology.The company’s pharmacovigilance and healthcare operations teams help pharmaceutical organizations maintain drug safety compliance, manage regulatory reporting, and ensure patient safety worldwide. By combining advanced technology with human expertise, Accenture continues to deliver innovative solutions that improve healthcare systems and pharmaceutical safety programs.FAQsQ1. What does a Pharmacovigilance Services Associate do?A Pharmacovigilance Services Associate monitors adverse drug reaction reports, processes safety cases, and ensures compliance with pharmacovigilance regulations.Q2. What qualifications are required for this role?Candidates should have a Bachelor’s or Master’s degree in Life Sciences or a BAMS degree.Q3. What experience is required?The position typically requires one to three years of experience in pharmacovigilance or drug safety operations.Q4. What technical knowledge is useful for this role?Knowledge of pharmacovigilance databases, MedDRA coding, WHO Drug Dictionary, and safety case processing workflows is beneficial.Q5. What career growth opportunities are available in pharmacovigilance?Professionals can progress to roles such as Senior Pharmacovigilance Associate, Drug Safety Specialist, Safety Scientist, or Pharmacovigilance Manager.Application Tips• Highlight pharmacovigilance or drug safety experience clearly in your resume.• Mention knowledge of MedDRA coding, safety databases, and adverse event reporting.• Emphasize medical writing and documentation skills.• Demonstrate your ability to follow regulatory guidelines and pharmacovigilance SOPs.• Include examples of safety case processing, drug safety monitoring, or regulatory reporting tasks.

Why This Role MattersPharmacovigilance plays a crucial role in ensuring the safety and effectiveness of medicines after they are released into the market. Professionals working in drug safety surveillance help detect, assess, and prevent adverse drug reactions that could impact patient health. This role directly supports pharmaceutical companies and regulatory bodies in maintaining high safety standards for medicines used worldwide.A Pharmacovigilance Services Associate is responsible for identifying and evaluating adverse event reports, maintaining safety databases, and ensuring that all drug safety information is handled according to international regulatory guidelines. By processing safety cases accurately and within required timelines, pharmacovigilance professionals contribute significantly to protecting patients and strengthening trust in healthcare systems.Job DescriptionA global professional services organization, Accenture, is seeking Pharmacovigilance Services Associates to support its pharmacovigilance operations and drug safety surveillance activities. This role involves managing safety case data, reviewing adverse event reports, performing medical coding, and ensuring regulatory compliance across global pharmacovigilance systems.The position focuses on handling Individual Case Safety Reports (ICSRs) and ensuring accurate documentation, evaluation, and submission of adverse event information in the global safety database. The associate will work closely with cross-functional teams, regulatory stakeholders, and internal safety teams to maintain high-quality pharmacovigilance standards. This opportunity is ideal for life sciences graduates who are interested in building a career in pharmacovigilance, drug safety operations, regulatory compliance, and pharmaceutical risk management.Key Features of the Role• Job Title: Pharmacovigilance Services Associate / Drug Safety Associate• Department: Pharmacovigilance Operations – Drug Safety Surveillance• Organization: Accenture• Experience Required: 1–3 years• Qualification: BAMS / Bachelor’s or Master’s Degree in Life Sciences• Industry: Pharmaceutical Safety & Healthcare Services• Work Environment: Global pharmacovigilance operations teamResponsibilitiesCase Intake and Case Processing• Identify and create safety cases in the global safety database from reports received through intake workflows, client mailboxes, electronic gateways, and other reporting sources.• Retrieve new safety information and follow-up correspondence for existing cases while maintaining compliance with company SOPs and regulatory requirements.• Perform triage, prioritization, and case processing activities for both serious and non-serious safety cases.Adverse Event Monitoring• Collect, review, and evaluate Adverse Event (AE), Serious Adverse Event (SAE), and Suspected Unexpected Serious Adverse Reaction (SUSAR) reports.• Ensure timely processing and evaluation of safety cases according to global regulatory timelines and internal service level agreements.• Perform duplicate checks and confirm the validity of Individual Case Safety Reports.Medical Coding and Safety Documentation• Conduct medical and drug coding for safety cases using standardized dictionaries such as MedDRA and WHO Drug Dictionary.• Draft detailed case narratives and document relevant clinical information based on available source data.• Maintain complete and accurate pharmacovigilance documentation for regulatory and internal review purposes.Regulatory Compliance and Reporting• Ensure all pharmacovigilance activities are performed according to regulatory requirements and company safety procedures.• Submit adverse event reports to global safety databases and regulatory authorities when required.• Monitor submissions and resolve issues related to report transmissions or database updates.Data Review and Quality Control• Review safety case data to ensure accuracy, completeness, and consistency across pharmacovigilance systems.• Validate safety data and correct discrepancies when necessary.• Monitor performance indicators and ensure that case processing meets defined quality standards and timelines.Operational Support and Collaboration• Coordinate with cross-functional teams, including regulatory affairs, clinical research, and safety operations teams.• Support audits, inspections, and compliance activities related to pharmacovigilance processes.• Assist with safety documentation, pharmacovigilance meeting minutes, and archival of safety records.Required Qualifications• Bachelor’s Degree in Life Sciences or related discipline.• Bachelor of Ayurvedic Medicine and Surgery (BAMS) or Master’s Degree in Life Sciences.• Basic knowledge of pharmacovigilance workflows and adverse event reporting processes.Educational RequirementsCandidates must hold one of the following qualifications from a recognized institution:• Bachelor’s Degree in Life Sciences• Master’s Degree in Life Sciences• Bachelor of Ayurvedic Medicine and Surgery (BAMS)These educational backgrounds provide the scientific and clinical knowledge required to understand adverse drug reactions, clinical terminology, and pharmacovigilance processes.Experience and SkillsExperience• 1–3 years of experience in pharmacovigilance operations or drug safety surveillance.• Experience handling Individual Case Safety Reports and safety database systems is preferred.Technical Skills• Familiarity with pharmacovigilance safety databases and case processing workflows.• Knowledge of medical coding dictionaries such as MedDRA and WHO-Drug.• Proficiency in Microsoft Office applications for documentation and reporting tasks.Professional Skills• Strong medical writing and documentation abilities.• Excellent communication skills in English (reading, writing, speaking, and listening).• Ability to work in a fast-paced environment and manage multiple safety cases simultaneously.• Strong attention to detail and analytical thinking.• Commitment to maintaining high standards of regulatory compliance.Salary InsightsPharmacovigilance professionals in India receive competitive compensation depending on experience, technical expertise, and role responsibilities. Entry-level associates with 1–3 years of experience can expect attractive salary packages along with opportunities for professional growth, training programs, and exposure to global pharmacovigilance operations.Company OverviewAccenture is one of the world’s leading professional services companies specializing in digital transformation, consulting, technology, and operations. The company operates in more than 120 countries and serves clients across multiple industries including healthcare, pharmaceuticals, finance, and technology.With a workforce of hundreds of thousands of professionals globally, Accenture combines advanced technology with human expertise to deliver innovative solutions. Its pharmacovigilance and healthcare operations teams support pharmaceutical companies in maintaining regulatory compliance, monitoring drug safety, and ensuring the protection of patient health worldwide.FAQsQ1. What does a Pharmacovigilance Services Associate do?A Pharmacovigilance Services Associate monitors and processes adverse drug reaction reports, maintains safety databases, and ensures compliance with global pharmacovigilance regulations.Q2. What qualifications are required for this position?Candidates should hold a Bachelor’s or Master’s degree in Life Sciences or a BAMS degree from a recognized institution.Q3. What experience is required for this role?The position typically requires 1–3 years of experience in pharmacovigilance, drug safety operations, or related pharmaceutical safety functions.Q4. What technical knowledge is important for this job?Knowledge of pharmacovigilance databases, MedDRA coding, WHO-Drug dictionaries, and safety reporting workflows is highly beneficial.Q5. What career growth opportunities exist in pharmacovigilance?Professionals can progress to roles such as Drug Safety Specialist, Senior Pharmacovigilance Associate, Safety Scientist, Pharmacovigilance Manager, or Regulatory Safety Expert.Application Tips• Highlight pharmacovigilance or drug safety experience clearly in your resume.• Mention knowledge of MedDRA coding, safety databases, or adverse event reporting.• Emphasize medical writing and documentation skills.• Demonstrate your ability to work with regulatory guidelines and compliance processes.• Include examples of safety case processing or pharmacovigilance project involvement.

Why This Role MattersPharmacovigilance professionals play a vital role in ensuring patient safety by monitoring, evaluating, and reporting adverse drug reactions. This role helps pharmaceutical companies and regulatory authorities maintain drug safety standards throughout a product’s lifecycle. By identifying adverse events, managing safety databases, and ensuring regulatory compliance, Pharmacovigilance Associates contribute significantly to protecting public health and improving medication safety worldwide.Job DescriptionA global professional services organization, Accenture, is hiring Pharmacovigilance Services Associates to support drug safety surveillance and case processing activities. The role involves managing Individual Case Safety Reports (ICSRs), reviewing adverse event data, performing medical coding, and ensuring compliance with international pharmacovigilance guidelines and regulatory timelines.This position is ideal for life science graduates who want to build a career in pharmacovigilance, drug safety monitoring, and regulatory compliance within the pharmaceutical and healthcare industry.Key Features of the Role• Job Title: Pharmacovigilance Services Associate / Pharmacovigilance Associate• Department: Pharmacovigilance Operations – Drug Safety Surveillance• Experience Required: 1–3 years• Qualification: BAMS / Bachelor’s or Master’s Degree in Life Sciences• Industry: Pharmaceutical Safety & Healthcare Services• Work Environment: Global pharmacovigilance operations team• Organization: AccentureResponsibilitiesCase Intake & Processing• Identify and create safety cases in the global safety database from multiple intake sources including client mailboxes, electronic gateways, and safety reporting systems.• Perform triage, prioritization, and data entry for serious and non-serious adverse event cases.• Process Individual Case Safety Reports (ICSRs) according to regulatory timelines and client SOPs.Adverse Event Monitoring• Collect, evaluate, and document adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs).• Perform duplicate checks and validate case authenticity in safety databases.• Assess seriousness, causality, and medical relevance of reported events.Medical Coding & Documentation• Perform medical coding using standardized dictionaries such as MedDRA and WHO Drug Dictionary.• Draft safety narratives for regulatory reporting and documentation.• Maintain accurate pharmacovigilance documentation and safety case records.Regulatory Compliance & Reporting• Ensure all pharmacovigilance activities comply with global regulatory requirements and company SOPs.• Submit safety reports to global safety databases and regulatory authorities.• Track regulatory submissions and troubleshoot submission-related issues.Data Management & Quality Assurance• Review safety data for accuracy, completeness, and consistency.• Monitor case processing quality metrics and ensure adherence to turnaround time (TAT) and KPIs.• Resolve pending action items, follow-ups, or clarifications related to safety cases.Collaboration & Operational Support• Coordinate with cross-functional teams, regulatory partners, and pharmacovigilance stakeholders.• Assist in pharmacovigilance audits, inspections, and compliance reviews.• Support pharmacovigilance projects, documentation archiving, and meeting coordination.Required Qualifications• Bachelor’s Degree in Life Sciences or equivalent.• Bachelor of Ayurvedic Medicine and Surgery (BAMS) or Master’s in Life Sciences.• Basic understanding of pharmacovigilance principles and drug safety processes.Educational RequirementsCandidates must possess one of the following degrees from a recognized institution:• Bachelor’s Degree in Life Sciences• Master’s Degree in Life Sciences• Bachelor of Ayurvedic Medicine and Surgery (BAMS)These qualifications provide the scientific knowledge required to understand adverse drug reactions, clinical terminology, and drug safety monitoring processes.Experience and SkillsExperience• 1–3 years of experience in pharmacovigilance or drug safety operations.• Experience handling ICSRs and safety database case processing is preferred.Technical Skills• Knowledge of safety databases and pharmacovigilance workflows.• Familiarity with medical dictionaries such as MedDRA and WHO-Drug.• Proficiency in Microsoft Office tools for documentation and reporting.Core Skills• Strong medical writing and documentation skills.• Excellent English communication skills (reading, writing, speaking, listening).• Ability to work in a fast-paced regulatory environment.• Strong analytical and problem-solving abilities.• High attention to detail and commitment to regulatory compliance.Salary InsightsPharmacovigilance Associates in India typically receive competitive salary packages based on experience and technical expertise. Compensation may include performance incentives, career development opportunities, and exposure to global pharmacovigilance operations.Company OverviewAccenture is a leading global professional services company with expertise in digital transformation, technology, consulting, and operations. The organization employs hundreds of thousands of professionals across more than 120 countries and delivers solutions that combine advanced technology with human ingenuity. Its pharmacovigilance and healthcare operations teams support pharmaceutical companies worldwide in maintaining drug safety, regulatory compliance, and patient protection.FAQsQ1. What is the primary responsibility of a Pharmacovigilance Associate?The primary responsibility is to monitor and process adverse drug reaction reports and maintain accurate safety records in compliance with regulatory standards.Q2. What qualifications are required for this role?Candidates must have a Bachelor’s or Master’s degree in Life Sciences or a BAMS degree.Q3. What experience level is required?The role requires 1–3 years of relevant pharmacovigilance or drug safety experience.Q4. What technical knowledge is useful for this role?Knowledge of MedDRA coding, WHO-Drug dictionaries, and pharmacovigilance safety databases is highly beneficial.Q5. What career growth opportunities exist in pharmacovigilance?Professionals can progress to roles such as Senior Drug Safety Associate, Pharmacovigilance Specialist, Safety Scientist, or Pharmacovigilance Manager.Application Tips• Highlight pharmacovigilance or drug safety experience in your resume.• Mention familiarity with MedDRA coding and safety databases.• Emphasize medical writing and documentation skills.• Include examples of adverse event case processing or safety monitoring tasks.• Demonstrate attention to regulatory compliance and quality standards.

Why This Role MattersThe Pharmacovigilance Services Specialist plays a critical role in ensuring patient safety through effective drug safety surveillance and regulatory compliance. This position oversees pharmacovigilance service delivery, ensuring high-quality case processing, risk management, and regulatory reporting aligned with global standards.By managing operational teams, mitigating risks, and ensuring timely submission of Individual Case Safety Reports (ICSRs), the role directly contributes to maintaining public trust in medicines and ensuring compliance with international pharmacovigilance regulations.Job DescriptionAccenture is hiring a Pharmacovigilance Services Specialist to oversee service delivery in drug safety surveillance operations. The selected candidate will manage pharmacovigilance case processing activities, coordinate with client project leads, oversee team performance, and ensure compliance with global regulatory requirements. The role may involve rotational shifts and interaction with internal and client stakeholders.Key Features of the Role• Position: Pharmacovigilance Services Specialist• Skill Area: Pharmacovigilance & Drug Safety Surveillance• Experience Required: 7–11 years• Qualification: B.Pharm / M.Pharm• Industry: Pharmacovigilance / Life Sciences Operations• Work Requirement: May require rotational shiftsKey ResponsibilitiesService Delivery & Team Management• Oversee end-to-end pharmacovigilance service delivery• Mobilize and manage resources to meet client requirements• Monitor team performance and ensure high-quality outputs• Manage risks, issues, and escalations with client and internal stakeholdersCase Processing & Drug Safety Operations• Manage case identification, data entry, and MedDRA coding• Oversee case processing, submissions, and follow-ups for ICSRs• Ensure compliance with global regulatory requirements and client guidelines• Maintain data accuracy in safety databasesRisk & Compliance Oversight• Support detection, assessment, and prevention of adverse drug effects• Ensure adherence to pharmacovigilance regulatory standards• Drive quality improvements and process optimization• Support compliance audits and regulatory inspectionsProblem Solving & Decision Making• Analyze and resolve moderately complex issues• Adapt existing methods to create improved solutions• Make decisions that impact team operations and service quality• Align team activities with strategic goals set by senior managementRequired QualificationsEducational Background:• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)Experience:• 7–11 years of experience in Pharmacovigilance / Drug Safety• Strong experience in ICSR case processing and regulatory submissions• Experience managing small teams or leading workstreamsCore Skills:• Strong analytical and problem-solving skills• Excellent written and verbal communication• Risk management and issue resolution capability• Collaboration and stakeholder management skills• Understanding of global pharmacovigilance regulationsSoft Skills:• Leadership and team coordination• Ability to work under deadlines• Client-facing communication skills• Adaptability in a dynamic environmentCompany OverviewAccenture is a global professional services organization with expertise in digital, cloud, security, strategy, consulting, technology, and operations. With over 784,000 employees serving clients in more than 120 countries, Accenture combines technology and human ingenuity to drive business transformation across industries. In the life sciences sector, Accenture supports pharmacovigilance services that ensure regulatory compliance, operational excellence, and patient safety.FAQsQ1. Is team management experience required?Yes, candidates should have experience managing small teams or workstreams.Q2. Is hands-on case processing experience necessary?Yes, strong exposure to ICSR case processing and MedDRA coding is required.Q3. Does the role involve client interaction?Yes, collaboration with client project leads and internal stakeholders is a key component.Q4. Are rotational shifts mandatory?Yes, this role may require working in rotational shifts.Q5. What experience level is expected?Candidates must have 7–11 years of pharmacovigilance experience.Application Tip• Highlight experience in ICSR case management and MedDRA coding• Showcase leadership or team management exposure• Mention regulatory submission and compliance experience• Demonstrate risk management and escalation handling examples• Include client-facing project coordination experience

Why This Role MattersThe General Dental Surgeon at DentArt Dental plays an important role in independently managing clinic operations while delivering quality general dental care. This position ensures responsible patient management, consistent treatment standards, and smooth day-to-day clinic functioning.Job DescriptionDentArt Dental is seeking a Full-Time General Dental Surgeon based in Mangadu, Chennai, Tamil Nadu. The role involves independently handling the clinic, providing general dental treatments, and maintaining high standards of patient care and responsibility. The ideal candidate should be a passionate BDS graduate, whether fresher or experienced, who is confident in managing clinical duties.Key Features of the Role• Position: General Dental Surgeon• Organization: DentArt Dental• Location: Mangadu, Chennai, Tamil Nadu• Employment Type: Full-Time• Salary Range: ₹15,000 – ₹18,000 per month• Experience Level: Freshers and Experienced candidates can applyResponsibilities• Independently manage and take responsibility for clinic operations• Diagnose and treat general dental cases• Provide quality patient care and consultation• Maintain proper clinical documentation and records• Ensure hygiene and sterilization protocols are followed• Manage patient appointments and workflow efficientlyRequired Qualification• Bachelor’s Degree in Dental Surgery (BDS)Educational Requirement• Bachelor’s Degree (Required)Important Requirements• Passionate and responsible approach to clinical practice• Ability to handle the clinic independently• Good patient communication skills• Commitment to maintaining hygiene and treatment standardsWhat We Offer• Salary ₹15,000 – ₹18,000 per month• Flexible work schedule• Opportunity to independently manage a clinic• Supportive working environmentExperience and Skills• Clinical experience in general dentistry (Freshers can apply)• Strong diagnostic and patient management skills• Responsible and self-driven work approach• Good documentation and record-keeping abilitySalary Insights• ₹15,000 – ₹18,000 per month• Flexible schedule benefit includedCompany OverviewDentArt Dental is a dental clinic based in Mangadu, Chennai, focused on delivering reliable general dental care. The clinic emphasizes responsibility, patient-centered treatment, and maintaining consistent clinical standards.FAQsWhat qualification is required?A Bachelor’s Degree in Dental Surgery (BDS) is required.Can freshers apply?Yes, both freshers and experienced candidates are eligible.Will I need to manage the clinic independently?Yes, the role requires taking individual responsibility for clinic operations.What is the salary offered?₹15,000 – ₹18,000 per month.Is there any additional benefit?Yes, a flexible work schedule is provided.Application Tips• Highlight your confidence in handling general dental procedures• Mention if you have independently managed cases or clinics• Emphasize responsibility and patient communication skills• Include internship or clinical exposure details if you are a fresher• State your availability to work in Mangadu, Chennai

Why This Role MattersThe Resident Dentist at Tiny Tusks Dental plays a vital role in delivering essential dental treatments while supporting specialist procedures. This position ensures quality patient care, accurate clinical documentation, and effective teamwork within the clinic, contributing to strong oral health outcomes and patient satisfaction.Job DescriptionTiny Tusks Dental is seeking a Full-Time Resident Dentist based in Korattur, Chennai, Tamil Nadu. The role involves diagnosing patients, delivering basic dental treatments such as oral prophylaxis and restorations, assisting senior consultants during specialty procedures, supervising auxiliary staff, and maintaining proper documentation. The ideal candidate should be confident in basic procedures and capable of effective patient communication.Key Features of the Role• Position: Resident Dentist• Organization: Tiny Tusks Dental• Location: Korattur, Chennai, Tamil Nadu• Employment Type: Full-Time• Salary Range: ₹15,000 – ₹30,000 per month• Experience Level: Minimum 1 year preferredResponsibilities• Diagnose and provide basic dental treatments (oral prophylaxis, restorations)• Assist senior consultants during specialty procedures• Educate patients on oral hygiene and post-operative care• Ensure strict adherence to treatment and post-op instructions• Maintain accurate documentation of all procedures performed• Supervise and guide colleagues and auxiliary staff• Ensure high standards of hygiene and patient careRequired Qualification• Bachelor’s Degree in Dental Surgery (BDS)Educational Requirement• Bachelor’s Degree (Preferred)Important Requirements• Minimum 1 year of total work experience (preferred)• Proficiency in Tamil and English (preferred)• Ability to reliably commute to Korattur, Chennai or relocate before joining• Strong communication skills• Confidence in performing basic dental proceduresWhat We Offer• Competitive monthly salary (₹15,000 – ₹30,000)• Hands-on exposure to specialty dental procedures• Opportunity to work alongside senior consultants• Supportive clinical learning environmentExperience and Skills• Clinical experience in basic dental treatments• Strong diagnostic and patient assessment skills• Good documentation and record-keeping ability• Effective communication in Tamil and English• Ability to supervise and coordinate with support staffAge Eligibility• Not specifiedSalary Insights• ₹15,000 – ₹30,000 per month• Salary may vary based on experience and clinical skillsCompany OverviewTiny Tusks Dental is a dental clinic located in Korattur, Chennai, focused on delivering quality dental care through a combination of general and specialty procedures. The clinic promotes patient education, ethical treatment, and collaborative teamwork among dental professionals.FAQsWhat qualification is required?A Bachelor’s Degree in Dental Surgery (BDS) is preferred.Is prior experience mandatory?A minimum of 1 year experience is preferred but may not be mandatory.What treatments will I handle?Basic treatments such as oral prophylaxis and restorations, along with assisting in specialty procedures.Is language proficiency required?Tamil and English proficiency is preferred.Is relocation required?Candidates must be able to commute reliably to Korattur, Chennai or relocate before joining.Application Tips• Highlight experience in oral prophylaxis and restorative procedures• Mention exposure to assisting in specialty cases• Include language proficiency (Tamil & English) clearly in your CV• Emphasize documentation and patient communication skills• State your ability to relocate or commute to Korattur

Why This Role MattersThe Medical Coder role at AS Medical Coding Tech is essential in transforming healthcare documentation into standardized diagnosis and procedure codes. This position supports accurate billing, insurance claims processing, and healthcare revenue cycle management by converting clinical information into ICD-10-CM and CPT codes.Job DescriptionAS Medical Coding Tech is hiring full-time, permanent Medical Billers/Coders for its locations in Karur, Gobichettipalayam, and Chennai. The role involves converting healthcare text information into numeric diagnosis and procedure codes using ICD-10-CM and CPT coding systems. Freshers and candidates with up to 1 year of experience in life sciences, paramedical, or medical backgrounds are encouraged to apply. Total openings: 450.Key Features of the Role• Position: Medical Biller / Coder• Organization: AS Medical Coding Tech• Location: Karur, Gobichettipalayam, Chennai• Employment Type: Full-Time, Permanent• Industry Type: Pharmaceutical & Life Sciences• Department: Healthcare & Life Sciences• Role Category: Health Informatics• Experience Required: 0 – 1 Year• Openings: 450• Salary: ₹3 – ₹3.5 LPAResponsibilities• Convert healthcare documentation into ICD-10-CM diagnosis codes• Assign CPT codes for medical procedures• Ensure accurate and compliant medical coding practices• Maintain confidentiality of patient health information• Support billing and revenue cycle management processes• Review clinical documentation for coding accuracyRequired Qualification• Any UG/PG in Life Sciences, Paramedical, or Medical fields• BPT / MPT / BDS / MBBS / BAMS / BHMS / B.Pharm / Nursing / Biotechnology / Microbiology and related fields eligibleEducational RequirementUG: BPT, B.Tech/B.E (Biotech/Biomedical), B.Pharm, BVSc, (Life Sciences Specializations), BUMS, MBBS, BDS, BHMS, BAMS and related fieldsPG: MPT, M.Pharm, (Life Sciences Specializations),(Biotech/Biomedical), MDS, MVSc and related fieldsImportant Requirements• Strong understanding of medical terminology• Interest in medical coding and billing processes• Attention to detail and accuracy• Basic computer knowledge• Willingness to work in healthcare revenue cycle managementEmployment Options• Large-scale hiring • Suitable for freshers and early-career professionalsWhat We Offer• Opportunity to enter the medical coding industry• Structured training in ICD-10-CM and CPT coding• Stable career in healthcare revenue cycle management• Competitive salary packageExperience and Skills• Knowledge of life sciences or paramedical background• Understanding of diagnosis and procedure coding• Analytical and documentation review skills• Strong focus on accuracy and compliance• Basic data handling and computer skillsSalary Insights• ₹3 – ₹3.5 Lakhs per annum• Salary based on qualification and performanceCompany OverviewAS Medical Coding Tech is an ISO 9001:2008 certified organization providing Medical Coding and Billing Services. The company has over 10 years of experience in revenue cycle management and supports healthcare providers with accurate coding and billing solutions.FAQsWho can apply?Any UG/PG candidate from life sciences, paramedical, or medical fields.Are freshers eligible?Yes, freshers and candidates with up to 1 year of experience can apply.What is the salary range?₹3 – ₹3.5 LPA.What coding systems are used?ICD-10-CM and CPT codes.How can I apply?Apply via Naukri using the link below or contact HR Shanmugapriya at 8072891550.Application Tips• Highlight medical or life sciences background clearly.• Mention knowledge of medical terminology.• Emphasize attention to detail and documentation skills.• Include any certification in medical coding if available.

Why This Role MattersThe Dental Surgeon at Perfect 32 Family Dental Solutions in Chennai provides essential dental care, ensuring patients receive high-quality oral treatment. This role supports clinic operations, patient assessment, and routine dental procedures, contributing to overall patient satisfaction and clinic efficiency.Job DescriptionPerfect 32 Family Dental Solutions is seeking a Dentist (freshers or with 2–3 years of experience) to manage the clinic on a full-time or part-time basis. The role involves patient assessment, performing basic dental procedures, and maintaining clinic standards.Key Features of the Role• Position: Dental Surgeon• Company: Perfect 32 Family Dental Solutions• Location: Chennai, Tamil Nadu, India• Employment Type: Full-Time / Part-Time• Salary: ₹7,000 – ₹15,000 per month• Work Setting: In-person clinic-based dental practiceResponsibilities• Assess patients’ oral health and provide dental care• Perform routine dental procedures• Manage clinic operations during working hours• Maintain accurate patient records and documentation• Ensure hygiene and sterilization protocols are followedRequired Qualification• BDS (Bachelor of Dental Surgery)Educational Requirement• Recognized BDS degree in IndiaImportant Requirements• Freshers or dentists with 2–3 years of experience• Ability to work full-time or part-time• Strong patient assessment and communication skillsBenefits and Culture• Flexible employment (full-time or part-time)• Opportunity to gain hands-on clinical experience• Supportive clinic environmentExperience and Skills• Freshers or 2–3 years of clinical experience• Patient assessment and basic dental procedure skills• Good interpersonal and communication abilitiesSalary Insights• ₹7,000 – ₹15,000 per month• Full-time or part-time options availableCompany OverviewPerfect 32 Family Dental Solutions in Chennai provides comprehensive dental care with a focus on patient satisfaction and clinical quality. The clinic supports dentists in skill development and maintains high standards for hygiene and patient care.FAQsWho can apply?Freshers or dentists with 2–3 years of experienceWhat is the salary range?₹7,000 – ₹15,000 per monthWhere is the job located?Chennai, Tamil Nadu, IndiaIs this full-time or part-time?Both full-time and part-time options availableHow do I apply?Apply via the link belowApplication Tips• Highlight BDS qualification and relevant experience• Emphasize patient assessment and basic dental procedure skills• Showcase reliability and ability to manage clinic hours

Why This Role Matters• The role of Pharmacovigilance Services Specialist ensures the safety and efficacy of medications through the monitoring and analysis of data from clinical trials, healthcare providers, and patients.• You will be instrumental in the detection, assessment, and prevention of adverse effects related to pharmaceutical products, impacting patient health and public trust in medications.Job Description• As a Pharmacovigilance Services Specialist, you will work within Accenture’s Life Sciences R&D vertical, spanning services across research labs, clinical trials, regulatory services, pharmacovigilance, and patient services solutions.• You will collaborate with biopharma companies to improve patient outcomes and ensure compliance with regulatory requirements.Key Features of the Role:• Full-time, on-site role based in Greater Chennai Area• Involves working on pharmacovigilance and patient services solutions• Key responsibilities include analyzing and reporting on adverse effects from clinical trials, healthcare providers, and patients• Ensures adherence to regulatory compliance and fosters public trust in medicationsResponsibilities• Analyze and solve moderately complex problems• Create new solutions leveraging existing methods and procedures• Understand and implement the strategic direction set by senior management• Collaborate with peers, clients, and Accenture management teams• Lead small teams or contribute as an individual contributor within AccentureRequired Qualifications• MBBSEducational Requirements:• Medical Degree (MBBS)Experience and Skills:• 0 to 4 years of experience in the relevant field• Ability to work in a team, adaptable, and flexible• Quick learning abilities and agility in new tasksAge Eligibility:• No specific age criteria mentionedSalary Insights• Competitive salary (not disclosed)Company Overview• Accenture is a global professional services company combining experience and specialized skills across digital, cloud, and security.• With 784,000+ employees in 120+ countries, Accenture offers services in Strategy & Consulting, Technology & Operations, and Accenture Song.• Accenture strives to create value and success for clients, employees, and communities by embracing the power of change.FAQs1 Is prior experience in pharmacovigilance required? No, this role is open to those with up to 4 years of experience.2 Does the role involve shift work? Yes, this role may require you to work in rotational shifts.Application Tips• Tailor your resume to highlight relevant experience and qualifications.• Emphasize your teamwork, adaptability, and quick learning abilities.

Why This Role MattersAccurate and complete documentation is the backbone of every successful clinical trial. Regulatory authorities require sponsors and CROs to maintain a well-organized Trial Master File (TMF) that demonstrates compliance with Good Clinical Practice (GCP), protocol adherence, and participant safety. Even minor documentation gaps can lead to inspection findings, compliance risks, or delays in regulatory approvals.The TMF Specialist I plays a foundational role in maintaining documentation quality and ensuring inspection readiness. At ICON plc, this position supports global clinical studies by contributing to document management activities, maintaining organized TMF structures, and ensuring adherence to both client and internal requirements. This role is ideal for professionals looking to strengthen their expertise in clinical documentation while building a long-term career in clinical research operations.Job DescriptionThe TMF Specialist I is responsible for supporting Trial Master File management activities across assigned projects. This role focuses on gaining familiarity with TMF structures, essential document requirements, document indexing, and compliance processes.Working closely with cross-functional teams, the TMF Specialist I assists in maintaining accurate and complete documentation within electronic document management systems. The role ensures that documentation activities align with client contracts, regulatory standards, and ICON procedures.This position requires strong attention to detail, organizational discipline, and a willingness to learn regulatory frameworks and documentation standards within a dynamic clinical research environment.Key Features of the Role• Entry-to-mid level opportunity within TMF Operations• Exposure to global clinical trial documentation processes• Hands-on experience with electronic document management systems• Cross-functional collaboration with Clinical Operations teams• Strong learning and development pathway• Foundation for career growth into TMF Specialist II, Senior TMF Specialist, or Clinical Operations roles• Compliance-focused and quality-driven environmentResponsibilities• Gain familiarity with Trial Master File (TMF) structure and essential document categories.• Assist in organizing, filing, and maintaining TMF documentation in electronic systems.• Ensure documents are uploaded, indexed, and classified correctly according to internal SOPs and client requirements.• Support ongoing document reconciliation and tracking activities.• Contribute to client services contracts and internal business requirements related to TMF management.• Verify document completeness and accuracy prior to filing.• Maintain audit-ready documentation standards under supervision.• Collaborate with Clinical Trial Managers, CRAs, and Regulatory teams to obtain required documents.• Follow established workflows for document review and approval processes.• Support quality checks to ensure compliance with ICH-GCP guidelines.• Assist in responding to internal queries related to document location and filing status.• Contribute to continuous improvement initiatives within TMF processes.Required Qualifications• Understanding or willingness to learn Trial Master File documentation standards.• Basic knowledge of clinical research processes preferred.• Strong organizational and document management skills.• High attention to detail and accuracy.• Ability to work within structured SOP-driven environments.• Effective communication skills for cross-team collaboration.• Ability to manage assigned tasks within defined timelines.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related scientific discipline.• Additional certification in Clinical Research or Regulatory Affairs is an advantage but not mandatory.Experience and Skills• 3+ years of prior experience in clinical research, document management, or related roles preferred.• Familiarity with electronic document management systems (eTMF systems preferred).• Basic understanding of ICH-GCP guidelines and regulatory documentation standards.• Experience supporting cross-functional teams in documentation activities.• Strong proficiency in Microsoft Office tools.• Ability to prioritize tasks and manage workload effectively.• Strong written and verbal communication skills.• Demonstrated ability to work effectively within a team environment.Salary InsightsCompensation for the TMF Specialist I role is competitive and aligned with entry-to-mid level clinical documentation positions within global CROs. Salary may vary depending on experience, skillset, and geographic location.In addition to base salary, employees at ICON plc may receive:• Health insurance coverage for employees and families• Retirement savings programs• Annual leave entitlements• Life assurance benefits• Global Employee Assistance Programme (LifeWorks)• Flexible country-specific optional benefits such as wellness initiatives and lifestyle programsICON’s total rewards structure is designed to support professional growth, financial security, and work-life balance.Company OverviewICON plc is a globally recognized healthcare intelligence and clinical research organization that partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of innovative therapies.Operating across multiple continents, ICON provides comprehensive clinical development services spanning early-phase trials through post-marketing research. The company emphasizes operational excellence, regulatory compliance, and scientific innovation.ICON fosters a diverse and inclusive workplace culture, committed to equal opportunity employment and accessible work environments. Professional development, collaboration, and continuous learning are central to the organization’s values.FAQs1. Is prior TMF experience mandatory?While prior TMF or document management experience is preferred, candidates with clinical research exposure and strong documentation skills are encouraged to apply.2. Is this role suitable for freshers?The role prefers candidates with some prior experience (3+ years), but relevant internships or document management exposure may be considered.3. Does this role involve regulatory inspections?The role supports inspection readiness activities but does not independently lead inspections at this level.4. What growth opportunities are available?Progression may include TMF Specialist II, Senior TMF Specialist, or broader Clinical Operations roles.5. Is system experience required?Familiarity with electronic document management systems is beneficial but can be developed on the job.Application Tips• Highlight any TMF, eTMF, or document management experience clearly.• Demonstrate understanding of GCP and regulatory documentation standards.• Showcase examples of accuracy and attention to detail in previous roles.• Mention experience working with cross-functional teams.• Emphasize organizational skills and ability to meet timelines.• Quantify experience where possible (number of studies supported, documents handled, etc.).

Why This Role MattersIn clinical research, documentation is the foundation of regulatory compliance and patient safety. Every clinical trial must maintain a complete and accurate Trial Master File (TMF) to demonstrate that the study was conducted in accordance with ICH-GCP guidelines and global regulatory requirements. Inspection readiness is not a one-time milestone it is a continuous process.At ICON plc, the Senior TMF Specialist plays a critical role in ensuring that essential documents are complete, properly indexed, and audit-ready throughout the study lifecycle. This role directly supports regulatory inspections, quality oversight, and operational excellence, contributing to the timely development of innovative therapies worldwide.Job DescriptionThe Senior TMF Specialist is responsible for overseeing electronic Trial Master File (eTMF) activities across assigned clinical studies. The position focuses on completeness reviews, missing document identification, metadata verification, and compliance monitoring within Veeva Vault.The role requires strong expertise in TMF structure, essential document requirements, and regulatory standards. The candidate must be detail-oriented, proactive in risk identification, and capable of managing multiple studies while adhering to agreed service level agreements (SLAs).Key Features of the RoleGlobal clinical trial exposureInspection readiness responsibilityAdvanced eTMF system involvement (Veeva Vault)Cross-functional collaboration with study teamsCompliance-driven and quality-focused environmentOpportunity for mentoring and training supportCareer progression into TMF Lead or Clinical Operations rolesResponsibilities• Perform comprehensive periodic and milestone-based eTMF completeness reviews.• Conduct cross-checks and co-dependency checks to ensure document alignment.• Identify missing, misfiled, or incomplete documents within Veeva Vault.• Maintain and update the Expected Document List (EDL) as required.• Ensure assigned studies remain inspection-ready at all times.• Apply ALCOEA principles to ensure documentation integrity and traceability.• Verify metadata accuracy and proper indexing within the system.• Ensure compliance with ICH-GCP guidelines and global regulatory requirements.• Support internal audits and regulatory inspections.• Proactively track overdue documents and escalate risks where necessary.• Collaborate with study teams to collect pending documents.• Monitor action items and ensure timely resolution within SLAs.• Maintain documentation tracking logs and review reports.• Provide training and guidance to internal teams on TMF best practices.• Participate in review meetings and communicate documentation gaps clearly.• Contribute to process improvements to enhance TMF efficiency and quality.Required Qualifications• Strong knowledge of Trial Master File structure and essential documents.• In-depth understanding of ICH-GCP and global regulatory standards.• Hands-on experience with electronic TMF systems (Veeva Vault preferred).• Excellent organizational and analytical skills.• Strong communication and stakeholder management abilities.• Ability to manage multiple clinical studies simultaneously.• High attention to detail and quality-focused mindset.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related scientific field.• Advanced degree preferred but not mandatory.• Clinical research or regulatory certifications are an added advantage.Experience and Skills• Minimum 7 years of TMF management experience.• 2–3 years of experience in missing document identification and resolution.• Experience conducting periodic and milestone-based TMF reviews.• Strong working knowledge of Veeva Vault eTMF system.• Proficiency in Microsoft Excel and document tracking tools.• Experience supporting inspection readiness initiatives.• Ability to interpret regulatory guidance and apply to documentation processes.• Proven track record of meeting SLAs and maintaining quality standards.Salary InsightsCompensation is competitive and aligned with industry benchmarks for senior-level TMF roles within global CROs. Salary varies based on experience, technical expertise, and geographic location.Benefits may include:• Comprehensive health insurance• Retirement planning programs• Performance-based incentives• Annual leave entitlements• Employee assistance programs• Flexible benefit optionsAt ICON plc, total rewards are designed to support professional growth, financial security, and work-life balance.Company OverviewICON plc is a leading healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies worldwide. The organization operates across multiple continents, delivering clinical development services that accelerate the availability of life-changing treatments.ICON fosters an inclusive and high-performance culture, encouraging collaboration, innovation, and continuous learning. Employees benefit from global exposure, structured career growth pathways, and a strong commitment to diversity and equal opportunity.FAQsIs Veeva Vault experience mandatory?It is highly preferred and considered a strong advantage.Does the role involve regulatory submissions?The focus is on TMF oversight rather than direct regulatory submissions.Is inspection readiness a key responsibility?Yes, ensuring inspection readiness is a core function of the role.What growth opportunities are available?Potential progression includes TMF Lead, Clinical Operations, or Quality Assurance roles.Application Tips• Clearly highlight TMF review and missing document identification experience.• Mention hands-on experience with Veeva Vault and eTMF systems.• Demonstrate knowledge of ALCOEA principles and ICH-GCP guidelines.• Quantify experience (number of studies supported, audits handled, etc.).• Showcase examples of stakeholder collaboration and SLA management.

Why This Role MattersThe Consultant Physiotherapist at Sparrc plays an important role in helping patients recover from musculoskeletal, neurological, and functional conditions through structured physiotherapy interventions. This position focuses on restoring mobility, reducing pain, and improving overall physical function. By providing evidence‑based rehabilitation care and personalised treatment plans, the role contributes to enhanced patient outcomes and long‑term wellness in the local community.Job DescriptionThe Consultant Physiotherapist will assess, diagnose, and treat patients with varied physiotherapy needs. Responsibilities include developing and implementing tailored treatment plans, delivering hands‑on therapy and exercise programs, educating patients on self‑management and preventive strategies, monitoring progress, and maintaining accurate clinical documentation. The role involves collaborating with multidisciplinary healthcare professionals to ensure comprehensive patient care.Key Features of the Role• Position: Consultant Physiotherapist• Company: Sparrc• Location: Porur, Chennai, Tamil Nadu, India• Employment Type: Full‑Time• Salary: ₹20,833+ per month (approximate)• Work Environment: Physiotherapy & Rehabilitation CentreResponsibilities• Conduct comprehensive assessments of patients’ musculoskeletal, neurological, and functional conditions• Develop and implement customised physiotherapy treatment plans• Provide hands‑on therapy, therapeutic exercises, and rehabilitation interventions• Educate patients on injury prevention, posture, movement, and exercises• Monitor patient progress and modify treatment plans as required• Maintain accurate clinical records and documentation• Collaborate with healthcare professionals to support holistic patient care• Ensure compliance with professional, ethical, and safety standardsRequired QualificationCandidates must hold a recognised physiotherapy qualification with clinical competence.Educational Requirement• Bachelor’s or Master’s degree in Physiotherapy (BPT/MPT)• Valid professional licensure/registration preferredImportant Remarks• Clinical experience in physiotherapy preferred, but fresh graduates may be considered• Strong communication and patient‑centred care skills required• Ability to work independently and as part of a multidisciplinary teamExperience and SkillsExperience Required• Experience in clinical physiotherapy preferred• Fresh graduates with strong academic and clinical training may be consideredKey Skills Expected• Proficiency in assessment, treatment planning, and rehabilitation techniques• Manual therapy and exercise prescription skills• Excellent patient education and counselling abilities• Professionalism, organisation, and accurate documentation• Collaborative teamwork and patient‑centred approachSalary Insights• ₹20,833+ per month (approximate) depending on experience• Compensation aligned with physiotherapy practice standards in ChennaiCompany OverviewSparrc in Porur, Chennai is a physiotherapy and rehabilitation centre providing evidence‑based treatment for a variety of physical conditions. The organisation focuses on personalised care, functional recovery, and patient education to support long‑term wellness and improved physical function.FAQs1. What qualification is required for this role?A Bachelor’s or Master’s in Physiotherapy (BPT/MPT) is required.2. Can fresh graduates apply?Yes, fresh graduates with strong clinical training may be considered.3. What type of patients will I work with?Patients with musculoskeletal, neurological, and functional rehabilitation needs.4. Where is the centre located?Porur, Chennai, Tamil Nadu, India.5. Is professional registration required?Professional licensure is preferred to practise physiotherapy.Application Tips• Highlight BPT/MPT qualification and any clinical internships or placements• Emphasise hands‑on therapy, assessment, and treatment planning skills• Showcase patient‑centred care and communication abilities• Include measurable treatment outcomes from previous roles or internships• Tailor your CV to reflect physiotherapy competencies, teamwork, and professional conduct

Roles and Responsibilities:• Diagnose and treat oral health conditions• Perform basic dental procedures and extractions• Provide preventive dental care advice to patients• Maintain accurate and updated patient records• Ensure proper hygiene and sterilization standards in the clinic• Deliver quality patient care with a professional approachQualification:• Bachelor’s or Doctorate degree in Dentistry (BDS or equivalent)• Valid dental license or certification as per regulatory requirementsExperience:• Clinical experience not mandatory• Freshers can applySkills:• Knowledge of general dental care and procedures• Ability to perform basic extractions and treatments• Good communication and interpersonal skills• Commitment to patient safety and hygiene standardsAbout the Company:RJ Dental Care is a dental clinic located in Periyar Nagar, Kolathur, Chennai, providing general dental treatments with a focus on patient care and maintaining hygiene standards.

Roles and Responsibilities:• Take responsibility for managing the clinic during evening hours.• Diagnose and treat patients with common dental conditions.• Perform dental procedures such as extractions, fillings, scalings, and other basic treatments.• Maintain accurate medical records and documentation.• Ensure proper patient care, hygiene, and infection control standards.• Demonstrate enthusiasm, professionalism, and hands-on clinical capability.Qualification:• Bachelor’s degree in Dentistry (BDS) or equivalent – Required.Experience:• Candidates with good hands-on clinical experience are preferred.• Salary negotiable based on skills and experience.Skills:• Patient assessment and clinical evaluation.• Proficiency in extractions, fillings, scalings, and basic dental procedures.• Knowledge of medical terminology and documentation.• Good communication and interpersonal skills.• Energetic, responsible, and passionate approach to patient care.About the Company:Nila Dental Clinic is a dental practice in Chennai focused on providing essential and preventive dental treatments. The clinic emphasizes patient-centered care, professional responsibility, and maintaining quality standards in everyday dental procedures.

Roles and Responsibilities:• Meet with patients to discuss and treat dental concerns.• Perform regular cleanings and other preventive dental procedures.• Carry out basic dental treatments and procedures.• Establish treatment plans to improve patients’ oral hygiene and dental health.• Manage and communicate effectively with other staff members to ensure quality patient care.• Maintain professionalism and deliver excellent patient interaction.Qualification:• Bachelor’s degree in Dentistry (BDS) or equivalent.Experience:• Experienced candidates and freshers with good communication skills can apply.Skills:• Strong interpersonal and communication skills.• Patient assessment and preventive care knowledge.• Ability to perform basic dental procedures.• Teamwork and coordination skills.• Professional attitude with a patient-centered approach.About the Company:Apollo Dental Clinic - Ambattur is part of Apollo’s dental care network, providing comprehensive oral healthcare services. The clinic focuses on quality treatment, preventive care, and maintaining high standards of patient satisfaction with a professional dental team.

Roles and Responsibilities:• Assist in diagnosing and treating patients’ dental conditions.• Handle patient care efficiently and provide preventive dental treatments.• Maintain accurate medical documentation and patient records.• Ensure adherence to clinic protocols and dental safety standards.• Demonstrate professionalism, responsibility, and patient-focused care.Qualification:• Bachelor’s degree in Dentistry (BDS) or equivalent.Experience:• Preferred total work experience of 1 year in a dental practice.Skills:• Patient assessment and clinical evaluation.• Knowledge of medical terminology and dental documentation.• Ability to maintain accurate medical records.• Strong responsibility, attention to detail, and professional ethics.About the Company:Tooth and Smile Dental Clinic is a dental practice in Chennai focused on providing comprehensive oral healthcare. The clinic emphasizes high-quality patient care, professional responsibility, and hands-on experience for its dental staff.

Roles and Responsibilities:• Assess and diagnose patients’ dental conditions accurately.• Provide dental treatments and preventive care as needed.• Maintain proper medical documentation and patient records.• Ensure compliance with clinic protocols and dental standards.• Demonstrate responsibility, professionalism, and dedication in patient care.Qualification:• Bachelor’s degree in Dentistry (BDS) or equivalent.Experience:• Basic knowledge and prior experience in dental practice is preferred but not mandatory.Skills:• Patient assessment and clinical evaluation.• Knowledge of medical terminology and documentation.• Ability to maintain accurate medical records.• Strong responsibility, attention to detail, and professional ethics.About the Company:RJ Dental Care is a dental clinic located in Perambur, Chennai, offering comprehensive dental services. The clinic focuses on patient-centered care, clinical responsibility, and delivering quality dental treatments in a professional environment.