Chennai Healthcare Jobs

Roles & Responsibilities • Manage clinical study documents in line with client, regulatory, and ICON requirements • Perform document receipt, review, quality checks, scanning, indexing, filing, and archiving in the Trial Master File (TMF) • Ensure continuous compliance with ICON SOPs, work procedures, and applicable regulatory guidelines • Collaborate with study teams, clients, and internal ICON departments to support study deliverables • Participate in internal and external audits and support inspection readiness activities • Prepare and maintain TMF status reports and tracking logs • Identify gaps or issues in TMF documentation and support corrective actions • Participate in training programs to enhance TMF and clinical research knowledge • Support special projects and additional responsibilities as assigned by the Manager Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences or related disciplines Experience • 1-15 years of experience in TMF management or clinical document management • Strong understanding of clinical trial documentation and TMF processes Skills • Strong oral and written communication skills • Excellent attention to detail and document accuracy • Good interpersonal and stakeholder coordination skills • Strong organizational and time management abilities • Working knowledge of clinical trial regulations and documentation standards About the Company ICON plc is a global leader in clinical research and healthcare intelligence, committed to advancing clinical development through innovation, partnership, and integrity, while fostering an inclusive work environment focused on improving patient lives worldwide.

Role & Responsibilities • Plan and execute scientific field activities for Rare Blood Disorders with focus on Hemophilia • Engage healthcare professionals through scientific discussions and evidence-based communication • Disseminate clinical study data, treatment guidelines and recent medical updates • Organize scientific meetings, CMEs and expert lectures in the therapeutic area • Support clinicians in diagnosis and management of hemophilia patients • Provide guidance on patient management pathways and real-world challenges • Collaborate in speaker training programs and scientific education initiatives • Collect field insights, treatment trends and share inputs for medical strategy • Align scientific field activities with company’s medical and brand strategies Qualifications • MBBS / MD or advanced scientific/medical degree Experience• 2–4 years of experience in Medical Affairs / MSL role • Prior experience in Hematology / Hemophilia is strongly preferred Skills • Strong scientific communication and presentation skills • Ability to engage and build long-term relationships with HCPs and KOLs • Knowledge of rare blood disorders, hemophilia and treatment guidelines • Strategic planning, analytical thinking and data interpretation abilities • Excellent interpersonal, teamwork and stakeholder management skills • Proficiency in English About the Company • Sanofi is a global healthcare leader dedicated to discovering, developing and delivering innovative medicines • The company focuses on advancing science in areas including rare diseases, vaccines, oncology and immunology

Role & Responsibilities:• Convert healthcare-related text information into numeric diagnosis and procedure codes• Assign accurate ICD-10 CM and CPT codes based on medical records and documentation• Review clinical documents to ensure coding accuracy and compliance• Maintain confidentiality and follow healthcare data protection standards• Work closely with billing and healthcare teams to ensure correct claim submission• Ensure coding meets regulatory and payer-specific guidelines• Maintain updated knowledge of coding standards and healthcare regulationsQualifications:• Any UG or PG degree in Life Sciences, Paramedical, or Medical fields• UG qualifications include B.Pharma, B.Sc (Biology, Microbiology, Biochemistry, Nursing, Chemistry, Botany, Food Technology, Optometry), BDS, BAMS, BHMS, BVSc, BUMS, MBBS, BPT (Biotechnology, Biomedical, Biochemistry)• PG qualifications include MPT,M.Pharma, M.Sc (Biotechnology, Biochemistry, Biology, Microbiology, Nursing, Zoology, Veterinary Science), MDS, MVSc, M.Tech (Biotechnology, Biomedical)Experience:• Freshers and experienced candidates can apply• Relevant medical coding or healthcare documentation experience will be an added advantageSkills Required:• Knowledge of ICD-10 CM and CPT coding systems• Medical coding and billing fundamentals• Understanding of medical terminology and healthcare processes• Attention to detail and analytical skills• Good communication and documentation skills• Ability to work in a team-oriented environmentKey Skills (Preferred):• Medical Coding• Pharmacy• Life Sciences• Paramedical• Nursing• Physiotherapy (BPT)• Microbiology• Biochemistry• Biotechnology• Biomedical Engineering• Nutrition and DieteticsAbout the Company:AS Medical Coding is an ISO 9001:2008 certified organization with over a decade of experience in revenue cycle management, providing specialized medical coding and billing services to healthcare organizations. The company focuses on accuracy, compliance, and quality-driven healthcare information management solutions.

Role & Responsibilities• Assess and diagnose patient physical conditions and rehabilitation needs• Develop and implement personalized treatment plans to improve mobility and overall well-being• Conduct physical evaluations and guide patients through therapeutic exercises• Provide hands-on therapy and monitor progress to adjust treatment plans accordingly• Maintain accurate patient records and document all treatments• Collaborate with other healthcare professionals for comprehensive patient care• Educate patients on exercises, posture, pain management, and lifestyle modificationsQualifications• Degree in Physiotherapy (BPT/MPT) from an accredited institution• Valid licensure or certification to practice as a Physiotherapist• Proficiency in physical therapy techniques, patient assessments, and therapeutic exercises• Strong knowledge of human anatomy, physiology, and rehabilitation principlesExperience• Previous experience in clinical or fitness/rehabilitation settings preferred• Freshers with strong skills and willingness to learn may also applySkills• Patient-centered approach with excellent interpersonal and communication skills• Ability to design and monitor individualized treatment plans• Collaborative mindset to work effectively within a healthcare teamAbout the CompanyACSES Fitness Studio is a professional healthcare and fitness organization based in Chennai, focusing on evidence-based physiotherapy, rehabilitation, and wellness services. The company is dedicated to delivering personalized care, supporting professional growth, and promoting long-term health and well-being for clients.

Roles & Responsibilities: • Academic teaching at UG/PG level • Curriculum development and academic planning • Guidance of students in research and projects • Participation in academic administration and quality assurance activities • Contribute to institutional research and accreditation processes • Perform duties assigned by the management from time to time Qualification: • M.Pharm (Master's of Pharmacy) with Ph.DExperience: • Assistant Professor (Pharmaceutics / Pharmaceutical Chemistry): Minimum 3 years • Professor (Pharmaceutics / Pharmaceutical Chemistry): Minimum 10+ years Skills: • Strong subject knowledge • Teaching and mentoring skills • Research orientation • Good communication and interpersonal skills About the Company: Sree Sastha Pharmacy College is committed to excellence in pharmaceutical education, research, and professional development, nurturing future-ready pharmacy professionals.

Role & Responsibilities: • Convert patient health information into standardized alphanumeric medical codes • Review medical reports including diagnoses, procedures, and prescriptions provided by healthcare professionals • Assign accurate diagnosis and procedure codes using ICD-10-CM and CPT coding systems • Ensure coding accuracy to support compliant medical claims and reimbursement processes • Maintain confidentiality and comply with HIPAA and healthcare regulations • Participate in quality checks and coding audits as required Qualification: • Any Paramedical Graduate or Post Graduate including Pharmacy, Physiotherapy, Nursing, B.O.T, or related disciplines Experience: • Freshers and experienced candidates are welcome Skills: • Knowledge of medical terminology and clinical documentation • Basic understanding of medical coding concepts • Good written and verbal communication skills • Strong attention to detail and analytical ability About the Company: Achievers Spot is a healthcare training and career development organization specializing in medical coding, billing, and healthcare IT services. The company focuses on equipping candidates with industry-relevant skills and certifications, enabling them to build successful careers in the growing healthcare services industry.

Role & Responsibilities: • Lead, manage, and motivate a regional sales team to achieve and exceed assigned business targets • Develop and implement effective regional sales strategies aligned with organizational goals • Drive market penetration, customer conversion, and brand visibility across assigned territories • Monitor sales performance, analyze market trends, and take corrective actions as required • Ensure consistent execution of promotional strategies and compliance with company guidelines • Build and maintain strong relationships with key customers, distributors, and stakeholders • Coach, train, and develop team members to enhance productivity and performance • Handle regional challenges proactively and provide effective problem-solving support • Support business growth through effective territory planning and resource utilization Qualification: • Bachelor’s degree in Pharmacy, Science, Management, or a related discipline- preferred Experience: • 5-10 years of experience in the pharmaceutical industry with a focus on sales or marketing • Experience in managing teams or aspiring ABMs with strong conversion and performance records • Senior ABM candidates with relevant experience may also apply • Minimum two years of consistency in the current or previous organization is required Skills: • Strong leadership, team management, and motivational skills • Strategic thinking with the ability to execute regional sales plans • Excellent communication and relationship-building abilities • Strong analytical skills for reviewing sales data and market trends • Effective problem-solving and decision-making capabilities • Experience in Gynecology products is an added advantage About the Company: ONEX LIFE SCIENCE is a growing pharmaceutical organization focused on delivering high-quality healthcare solutions across key therapeutic segments. With a commitment to ethical practices, innovation, and customer-centric growth, the company provides a dynamic work environment that encourages leadership development, performance excellence, and long-term career progression.

Job Role & Responsibilities• Assist dentists during daily procedures• Prepare and sterilize instruments and treatment rooms• Support patient care and comfort during treatments• Maintain cleanliness and hygiene in the clinic• Follow instructions and clinic protocols carefully• Willingness to learn and adapt to clinic operationsQualifications• 10th pass / 12th pass / Any degree or diplomaExperience• Fresher or experienced candidates can applySkills Required• Basic understanding of dental procedures• Good communication in Tamil and basic English• Punctual, hygienic, and patient-friendly• Willingness to learn and work in a teamAbout the Company• Dental clinic providing quality oral care• Supportive environment with learning opportunities• Focus on hygiene, patient care, and professional growth

Job Role & Responsibilities• Perform basic dental procedures including crown cutting, RCTs, and delivery• Diagnose patients and plan appropriate dental treatments• Assist in surgical procedures and OT duties when required• Maintain accurate patient records and follow hospital protocols• Communicate treatment plans clearly and professionally• Willingness to work, learn, and grow in a multispeciality hospital environmentQualifications• BDS or MDS from a recognized dental institution• MDS freshers can applyExperience• 0–3 years of clinical experience• Minimum 3 years preferred but not mandatorySkills Required• Strong clinical skills• Excellent communication and patient-handling abilities• Ability to perform basic dental procedures independently• Willingness to learn and adapt• Team-oriented and professional approachAbout the Company• Reputed multispeciality hospital• Provides excellent clinical and surgical exposure• Equipped with modern infrastructure and OT facilities• Supportive and learning-focused work environment

Role & Responsibilities • Perform case intake and processing of Individual Case Safety Reports (ICSRs) • Handle Adverse Event (AE) and Serious Adverse Event (SAE) data • Code medical terms using MedDRA and WHO-DD • Perform quality checks on safety case data • Support global drug safety and compliance activities • Work on post-marketing surveillance and COVID-related safety data • Ensure adherence to ICH-GCP, GVP, and regulatory timelines Qualifications & Experience • B.Pharm, M.Pharm, BSc / MSc Life Sciences • Freshers with internship or project exposure in Pharmacovigilance, Clinical Research, Drug Safety, or COVID safety projects Skills • Basic understanding of pharmacovigilance concepts • Good communication and documentation skills • Willingness to work in rotational shifts About the Company • Accenture supports global pharmaceutical clients through structured pharmacovigilance and drug safety operations, offering corporate exposure and stable career growth

Role & Responsibilities • Conduct oral exams, diagnose conditions, and develop personalized treatment plans. • Perform treatments such as fillings, extractions, root canals, and applying sealants. • Educate patients on brushing, flossing, diet, and provide preventive care like cleanings. • Interpret diagnostic tests such as X-rays and refer to specialists when needed. • Administer anesthetics and prescribe antibiotics or pain relief medications. • Supervise dental assistants and hygienists, maintain accurate patient records, and ensure adherence to standards. • Perform surgical procedures on teeth, gums, and jawbones. Qualifications & Experience • Proven experience as a dentist. • Expertise in performing dental treatments and surgeries. • Strong knowledge of dental practices, innovations, and tools. • Excellent communication and patient care skills. Why Join Us? • Opportunity to work in a dynamic and supportive environment. • Growth potential and exposure to the latest dental practices.

Role & Responsibilities • Assist in the coordination and administration of clinical trials • Ensure compliance with study protocols and regulatory requirements • Maintain and organize clinical trial documentation and regulatory submissions • Support preparation of study-related materials such as informed consent forms and case report forms • Collaborate with cross-functional teams for smooth trial execution • Track and report clinical trial metrics and milestones to management Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or healthcare-related field Experience • Freshers or candidates with prior experience in clinical trials Skills • Strong understanding of GCP guidelines and clinical trial processes • Excellent organizational, communication, and multitasking skills • Ability to work in a fast-paced, collaborative environmentPerks & Benefits • Comprehensive health insurance plans for employees and families • Competitive retirement and savings plans • Generous annual leave and flexible working options • Global Employee Assistance Program (TELUS Health) • Country-specific benefits (gym memberships, travel passes, childcare vouchers) • Inclusive workplace fostering diversity, equity, and belonging About the Company • ICON plc, a global leader in healthcare intelligence and clinical research • Provides cutting-edge solutions in clinical development • Offers a supportive and inclusive workplace focused on career growth

Role & Responsibilities • Manage and lead a team of Medical Reviewers • Allocate work, monitor productivity and review assignments • Perform quality review of medical record summaries in client-specific formats • Train and onboard new team members • Handle client communication via email and coordination calls • Ensure timely and accurate delivery of assigned projects • Plan and support cross-training initiatives • Maintain compliance with internal quality and documentation standards Qualification • MBBS • MD / MS / Doctorate in any specialization Experience • 5 – 10 years of relevant medical review / healthcare documentation experience Skills • Team management and leadership • Medical record summarization and quality review • Client communication and coordination • Training and mentoring • Strong documentation and analytical skills About the Company The organization provides specialized medical review and clinical documentation services supporting global healthcare and life sciences clients with high-quality medical data review and compliance solutions.

Role & Responsibilities • Engage Thought Leaders (Doctors) through scientific exchange, education and data     dissemination • Provide on-label scientific communication and handle unsolicited off-label queries in compliance with regulations • Support and participate in Medical Society interactions and Advisory Boards • Attend congresses and conventions to build relationships and gather competitive intelligence • Plan and conduct scientific training programs and educational events • Identify, profile and segment Thought Leaders and support engagement strategy • Prepare reports and track field activities against objectives • Provide external scientific training and educational support as requiredQualification • MD / MBBS / BAMS / BDS / MDS • Degree in Natural Sciences (Life Sciences / Pharmacy / Biomedical) Required Skills • Knowledge of Women’s Health, Contraception, Endometriosis therapy areas • Understanding of clinical trials and study design • Excellent presentation, communication and scientific writing skills • Ability to work independently and in cross-functional teams • Strong relationship building and stakeholder management skills

Key Responsibilities • Oversee adherence to Quality Management Framework procedures to ensure delivery of high-quality pharmacovigilance cases • Review and improve project Quality Management Systems and suggest process enhancements • Collaborate with Team Leads, Trainers and Medical Reviewers to implement new or enhanced quality processes • Coordinate with Quality Reviewers to maintain compliance with quality standards • Review late logs, perform Root Cause Analysis (RCA) and define Corrective and Preventive Actions (CAPA) • Ensure timely documentation and closure of late logs as per client SOPs • Conduct training, refresher sessions and awareness programs on case processing conventions • Work with Operational Excellence and Capability Development teams to enhance engagement quality • Support audits, inspections, SOP development and maintenance • Review safety case data for completeness and accuracy • Track, submit and distribute quality and compliance reports • Maintain client mailboxes, SharePoint, databases and safety tools • Drive zero quality deviations leading to regulatory submission delays • Support transitions, documentation archiving, and cross-functional coordination Skills & Competencies • Working knowledge of ICH, GCP, FDA, MHRA and global PV regulations • Strong attention to detail and data accuracy • Good understanding of medical terminology • Strong verbal and written communication skills • Proficiency in MS Excel, Word and PowerPoint • Strong interpersonal and stakeholder management skillsAbout Accenture Accenture is a global professional services company delivering Strategy & Consulting, Technology and Operations services across more than 120 countries. With industry-leading capabilities in digital, cloud and security, Accenture supports global life sciences clients through advanced technology and intelligent operations centers.

Role & Responsibilities • Collect, assess, and investigate adverse events, product malfunctions, and complaints related to medical devices • Prepare and submit MDV reports to CDSCO, US FDA, and EU authorities • Maintain documentation for recalls, FSCAs, risk assessments, and CAPA implementation • Handle end-to-end complaints management and audit support • Monitor and report ADRs from spontaneous reports, literature, and clinical trials • Prepare and submit ICSRs, PSURs, and DSURs • Perform signal detection, trend analysis, and risk–benefit assessments • Execute Post-Marketing Surveillance (PMS) activities • Ensure compliance with global PV and MV regulatory requirements Qualification • B.Pharm / M.Pharm Experience • 1–6 years in Pharmacovigilance or Medical Device Vigilance Skills • Strong knowledge of global PV and MDV regulations • ICSR, PSUR, DSUR preparation • Complaints handling and CAPA management • Audit readiness and regulatory compliance • Good communication and documentation skills About the Company Appasamy is a leading medical device and pharmaceutical organization known for its high-quality ophthalmic products and strong commitment to patient safety, regulatory compliance, and innovation in healthcare solutions.

Role & Responsibilities Perform end-to-end ICSR processing for AE, SAE and SUSAR cases Identify, triage and create cases in global safety databases Review source documents for validity and medical relevance Perform MedDRA and WHO-Drug coding Draft case narratives and E2B sender comments Manage follow-ups, reconciliations and regulatory timelines Support audits, inspections and pharmacovigilance projects Handle literature intake, mailbox monitoring and translations Qualification B.Pharm BSc Nursing Bachelor’s Degree in Life Sciences Experience 0–1 year (Freshers eligible) Skills Basic knowledge of pharmacovigilance and ICSR workflows Familiarity with MedDRA and WHO-Drug Good documentation and MS Office skills Strong English communication skills Ability to work in compliance-driven environmentsAbout the Company Accenture is a global professional services leader operating in over 120 countries Delivers technology-driven healthcare and life sciences solutions Provides structured career growth and global exposure in pharmacovigilance

Role & Responsibilities Perform end-to-end ICSR case processing Triage, prioritize and assess adverse event cases Conduct MedDRA and WHO-Drug coding Assess seriousness, causality and expectedness Draft narratives and sender comments Manage follow-ups, reconciliations and regulatory timelines Support inspections, audits and safety surveillance activities Handle literature review and mailbox management Qualification Bachelor of Ayurvedic Medicine and Surgery (BAMS) Bachelor’s Degree in Life Sciences Master’s Degree in Life Sciences Experience 1–3 years of pharmacovigilance experience Skills Strong knowledge of pharmacovigilance workflows Good command over MedDRA and WHO-Drug coding Medical writing and documentation skills Proficiency in MS Office tools Excellent communication and compliance orientationAbout the Company Accenture is a global professional services organization with large-scale life sciences operations Works with international clients and regulatory frameworks Offers long-term growth in drug safety and pharmacovigilance careers

About role & responsibilities • Perform advanced medical coding of diagnoses, procedures and medications • Code clinical trial data using MedDRA and WHO Drug dictionaries • Ensure accuracy, consistency and regulatory compliance across studies • Resolve complex coding discrepancies and medical queries • Collaborate with clinical, safety and data management teams • Support development and refinement of medical coding SOPs and conventions • Stay updated with global medical coding standards Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Healthcare or related field Skills • Strong working knowledge of MedDRA and WHO Drug • Understanding of clinical trial processes and regulatory requirements • High attention to detail and analytical problem-solving skills • Ability to work in cross-functional global teams • Good documentation and communication skills Experience • Proven experience in medical coding within clinical research Salary • ₹6,00,000 – ₹10,00,000 per annum (estimated) Benefits • Comprehensive health insurance for employee and family • Competitive leave entitlements • Retirement and long-term savings plans • Employee Assistance Programme (24/7 wellbeing support) • Life insurance coverage • Flexible benefits – childcare support, gym discounts, travel subsidies and health assessments • Hybrid / office-with-flex work model About the company • ICON plc is a global leader in healthcare intelligence and clinical research • Provides global clinical trial, regulatory and medical coding solutions