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Roles & Responsibilities• Act as account lead or primary internal/external contact for standalone coding studies or accounts• Manage customer relationships, including coding-related negotiations on timelines, budgets, and scope• Provide leadership and senior support to Lead Coders on large, global clinical studies• Serve independently as Lead Data Coder and/or Coding Reviewer for multiple projects• Perform the role of Data Operations Coordinator (DOC), Data Team Lead (DTL), or customer site lead as required• Manage and oversee quality control procedures across studies• Perform and oversee Serious Adverse Event (SAE) reconciliation activities• Collaborate with customers to develop solutions and action plans for issues, risks, and escalations• Proactively identify quality risks and ensure on-time project delivery• Identify and manage out-of-scope activities and conduct due diligence• Manage project team resource planning and capacity• Mentor and train team members to build coding and CDM expertise• Drive process improvements, best practices, and quality initiatives within CDM and coding functions• Support development and implementation of new technologies• Participate in or present at local and international scientific forums• Contribute expert input to development and maintenance of SOPs and work instructions• Ensure effective communication and collaboration with CDM teams and client stakeholdersQualification• Qualification in Pharmacy, Dental, Medical, Nursing, Life Sciences, or related field• High School Diploma with relevant experience may be considered as per role requirementsExperience• Minimum 7 years of relevant experience in clinical trials within data management and/or coding• Proven experience managing multiple global studies, complex customer negotiations, and bid defense meetingsSkills• Expert knowledge of medical dictionaries (MedDRA, WHODD, ICD-9, etc.)• Strong understanding of medical terminology, pharmacology, anatomy, and physiology• Advanced knowledge of clinical data management processes and systems• Excellent understanding of clinical drug development processes• Strong leadership, team management, and mentoring skills• Excellent project management, organizational, and communication skills• Sound financial management and budgeting knowledge• Ability to make independent decisions and manage cross-functional teams effectivelyAbout the OrganizationIQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, helping life sciences companies accelerate the development and commercialization of innovative medical treatments to improve patient and population health worldwide.
Roles & Responsibilities• Serve independently as Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) for one or more protocols• Manage delivery of coding activities and standalone coding projects across the study lifecycle• Validate and test coding applications, reports, datasets, edits, and coding-related programming activities• Perform comprehensive data review, write and resolve data clarifications• Manage coding-related timelines with guidance from DOC, Data Team Lead (DTL), or Manager• Perform Serious Adverse Event (SAE) reconciliation activities• Act as backup for Lead Coder, DOC, or DTL when required• Execute quality control procedures and support implementation of new technologies• Provide independent coding and project-related solutions to the Data Management team• Handle audit and inspection requirements for assigned studies• Ensure compliance with SOPs, work instructions, and regulatory requirements• Maintain effective communication and working relationships with internal teams and stakeholdersQualification• Degree in Pharmacy, Dental, Medical, Nursing, Life Sciences, or related field• LPN (Licensed Practical Nurse) – State Licensure (where applicable)Experience• Minimum 2 years of relevant experience in clinical data management and/or medical coding• Equivalent combination of education, training, and experience may be consideredSkills• Strong knowledge of medical terminology, pharmacology, anatomy, and physiology• In-depth experience with medical dictionaries (MedDRA, WHODD, etc.)• Understanding of end-to-end clinical data management processes• Excellent attention to detail and problem-solving ability• Good understanding of database technologies related to data management and coding• Strong written and verbal communication skills in English• Ability to work independently and collaborate effectively with cross-functional teamsAbout the OrganisationIQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, enabling life sciences organizations to accelerate the development and commercialization of innovative treatments that improve patient outcomes worldwide.
Roles & Responsibilities• Perform medical surveillance and pharmacovigilance case processing activities• Review, assess, and medically code adverse event reports• Conduct medical review of ICSRs (Individual Case Safety Reports)• Ensure compliance with regulatory requirements and internal SOPs• Support signal detection activities and safety data analysis• Maintain accurate documentation, reporting, and audit readinessQualification• Pharm D (Doctor of Pharmacy)• BDS / MDS• BHMS• BAMSExperience• Fresh graduates eligibleSkills• Good understanding of medical terminology• Strong analytical and assessment skills• Effective communication and documentation abilities• Interest in pharmacovigilance, drug safety, and medical surveillanceAbout the OrganizationIQVIA – A global human data science company providing advanced analytics, technology solutions, and clinical research services, offering hybrid work opportunities and global exposure in pharmacovigilance and drug safety.Interested and eligible candidates can send their updated resume to: Email: pavan.cm@iqvia.com
Roles & responsibilities:• Assess clients’ health and wellness needs and create personalized wellness plans• Guide clients on implementing strategies that promote long-term health and vitality• Educate clients on recovery techniques, performance enhancement, and lifestyle changes• Monitor client progress to ensure optimal outcomes• Deliver exceptional customer service and maintain client relationshipsQualifications:• MBBS or Bachelor’s degree or equivalent experience in a health-related discipline• Background in nutrition, physiotherapy, exercise science, or related field is a plusExperience:• Not specifiedSkills required:• Strong knowledge and experience in health and wellness, longevity strategies, and recovery therapies• Excellent communication, client engagement, and interpersonal skills• Ability to assess individual needs and design personalized wellness and performance plans• Enthusiasm for promoting long-term health and optimizing performanceAbout the company:Evity Wellness is a social wellness club offering next-generation recovery and performance therapies to help individuals build strength, stay healthy, recover fully, and achieve peak performance. The company focuses on long-term vitality and wellness for improved daily living.
Roles & Responsibilities:• Review, assess, and process safety data in compliance with regulatory requirements.• Perform pharmacovigilance activities including AE intake, triage, and case processing.• Enter and manage safety cases in safety databases with accurate documentation.• Perform MedDRA coding, product coding, and narrative writing.• Handle literature case processing and follow-up activities.• Ensure adherence to SOPs, internal guidelines, and quality standards.• Meet defined productivity, quality, and turnaround time metrics.• Attend project meetings and escalate issues to senior team members when required.• Complete mandatory trainings within defined timelines.Qualification:• Bachelor’s degree in Pharmacy, Life Sciences, or a related healthcare discipline• B. Pharm / M. Pharm (Preferred)Experience:• Freshers interested in Drug Safety / Pharmacovigilance• Prior exposure or interest in Pharmacovigilance / Drug Safety will be an advantageSkills:• Good knowledge of medical terminology• Strong written and verbal communication skills• Working knowledge of MS Office and web-based applications• High attention to detail and time management skills• Ability to work independently and within a team• Willingness to work in shiftsAbout the Organization:IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare intelligence, providing advanced analytics, technology solutions, and clinical services to the life sciences industry, and offering strong career growth opportunities for professionals entering the drug safety and regulatory domain.
ROLE & RESPONSIBILITIES:• Assess children’s developmental needs using standardized occupational therapy tools• Plan and implement individualized therapeutic intervention programs• Address developmental delays and disabilities through structured therapy sessions• Monitor, evaluate, and document patient progress regularly• Collaborate with parents, caregivers, educators, and multidisciplinary teams• Provide guidance and support to families for consistent home-based interventions• Maintain detailed and accurate therapy records and reports• Support professionals through guidance and collaborative care planningQUALIFICATION:• Degree or certification in Occupational Therapy or a related field• Valid registration/licensure as per professional requirementsEXPERIENCE:• Experience working with children with developmental delays or disabilities is preferredSKILLS:• Strong expertise in Occupational Therapy and Rehabilitation• Knowledge of Pediatrics and child development• Excellent communication and interpersonal skills• Empathy, patience, and ability to build rapport with children and families• Ability to work effectively within multidisciplinary teamsABOUT THE COMPANY:Mom’s Belief is a child-focused organization committed to holistic development through early awareness and targeted intervention. Using a multidisciplinary approach, standardized clinical methods, and flexible online and offline programs, Mom’s Belief empowers children with developmental delays and disabilities to achieve their full potential while supporting parents, educators, and caregivers at every step.
Role & Responsibilities• Perform end-to-end pharmacovigilance case processing (ICSRs) in line with global regulations• Handle case intake, data entry, medical coding, quality review, and case lifecycle management• Work extensively on the Argus Safety Database for safety case processing• Ensure compliance with ICH-GCP, SOPs, and regulatory timelines• Maintain high accuracy, data quality, and audit readiness in safety reporting• Collaborate with cross-functional and global PV teams• Support timely delivery of pharmacovigilance activities and safety operationsQualification• B.Pharm / M.Pharm / Pharm.DExperience• 1 to 5 years of relevant pharmacovigilance case processing experience• Immediate joiners preferredSkills• Mandatory hands-on experience with Argus Safety Database• Strong knowledge of pharmacovigilance regulations and workflows• High attention to detail and quality orientation• Good communication and documentation skillsAbout the Company• IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare analytics, Supports pharmaceutical and biotech companies with end-to-end drug development services
Roles & Responsibilities• End-to-end PV case processing (ICSRs) in compliance with global regulatory standards• Performing case intake, data entry, medical coding, and quality review• Working extensively on the Argus Safety Database for case lifecycle management• Ensuring compliance with ICH-GCP, SOPs, and regulatory timelines• Collaborating with cross-functional global PV teams• Maintaining high accuracy and audit readiness in safety dataQualification• B.Pharm / M.Pharm / PharmDExperience• 1–5 years of relevant pharmacovigilance case processing experience• Hands-on experience with Argus Safety DatabaseSkills• Strong attention to detail• Good communication and documentation skills• Ability to join immediatelyAbout the OrganizationIQVIA is a global leader in clinical research and pharmacovigilance services, providing innovative solutions and trusted expertise across the life sciences industry. The company offers a structured work environment with exposure to global PV operations and opportunities for professional growth.📧 Send your updated CV to: heena.gill@iqvia.com
ROLES & RESPONSIBILITIES:• Diagnose oral health conditions and plan appropriate dental treatments• Perform general dental procedures including fillings, extractions, root canals, and crown placements• Educate patients on oral hygiene, preventive care, and treatment plans• Maintain accurate and up-to-date patient records• Collaborate with other dental professionals to provide comprehensive patient care• Ensure a clean, safe, and hygienic clinical environment in compliance with health regulationsQUALIFICATIONS:• DDS / DMD (or BDS equivalent) from a recognized institution• Valid license to practice dentistry in the respective state/regionEXPERIENCE:• Prior clinical experience preferred• Experience with modern dental technologies is an added advantageSKILLS REQUIRED:• Strong diagnostic and clinical skills• Excellent communication and interpersonal abilities• Attention to detail and manual dexterity• Knowledge of infection control and safety protocols• Willingness to continuously learn and adapt to new dental techniquesPREFERRED SKILLS:• Specialization in Orthodontics, Periodontics, or Pediatric Dentistry (not mandatory)ABOUT THE COMPANY:Doctor Tooth Dental Clinic is a patient-focused dental care provider in Kolkata, committed to delivering high-quality dental treatments in a safe, professional, and hygienic environment. The clinic emphasizes comprehensive care, modern dental practices, and a positive patient experience.
Role & Responsibilities • Exchange and disseminate scientific, educational, and research-related information with Thought Leaders (TLs) proactively and reactively • Provide clarification and education of scientific data, study protocols, meeting abstracts, and professional literature, both on-label and off-label, in alignment with local regulations • Answer medical/scientific queries from Medical Societies regarding Bayer products • Organize, support, and participate in advisory boards • Attend congresses and conventions, interact with TLs, establish new contacts, and gather competitive intelligence • Plan and organize scientific education and training events with TLs within specific therapeutic areas or products • Contribute to internal understanding of specific TL interests and expertise within the medical community • Submit timely reports and track activities against agreed objectives • Provide external scientific support, training, and education where needed Qualification • Qualification in natural sciences or a medical background (MD, MBBS, BAMS, BDS, MDS) Experience • Basic knowledge of the concerned therapy area and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and within a team environment • Ability to build productive relationships both internally and externally Skills • Excellent presentation and written and verbal communication skills • Ability to engage and influence thought leaders and stakeholders effectively • Proficiency in managing scientific data and presenting it clearly to diverse audiences About The Company • Bayer – A global leader in life sciences, Bayer is dedicated to driving innovation and improving lives through advanced solutions in healthcare and agriculture. The company values dynamic shared ownership (DSO) and fosters a work environment that prioritizes higher productivity, faster innovation, and better results. Bayer is committed to diversity and inclusivity, promoting fairness and respect at work.
Role & Responsibilities • Dispense medicines as per prescriptions issued by authorised medical officers • Maintain proper storage, handling, and inventory of drugs and medical supplies • Ensure compliance with drug safety, expiry checks, and quality standards • Maintain pharmacy records, registers, and documentation • Assist in procurement, receipt, and stock verification of medicines • Support healthcare services provided within the institute • Follow institutional rules, SOPs, and government regulations Qualification • Degree or Diploma in Pharmacy from a recognised institution • Registration with State Pharmacy CouncilPay Level: Level 5 (7th CPC) Vacancies: 1 (UR) Experience • Relevant experience in hospital, institutional, or clinical pharmacy preferred • Government or autonomous institute experience desirable Skills • Knowledge of drug storage, dispensing, and inventory management • Attention to detail and record-keeping accuracy • Understanding of pharmacy laws and regulations • Ability to work independently and in coordination with healthcare staff • Basic computer skills for documentation and reporting About the Organisation • Indian Statistical Institute (ISI) is an Institute of National Importance, Funded by the Ministry of Statistics & Programme Implementation, Government of India
Roles & Responsibilities:• Assess patients’ physical conditions and rehabilitation needs• Plan and execute physiotherapy treatment programs• Support patient recovery and rehabilitation through therapeutic exercises and interventions• Maintain accurate patient records and progress reports• Collaborate with doctors and other healthcare professionals for holistic patient care• Educate patients on preventive care and post-treatment exercisesQualifications:• Bachelor’s Degree or Diploma in Physiotherapy (BPT/DPT)• Valid registration with the relevant physiotherapy councilExperience:• Freshers or experienced candidates may applyKey Skills:• Strong knowledge of physiotherapy principles and rehabilitation techniques• Patient-handling and communication skills• Ability to work in a hospital or clinical environment• Compassionate and ethical approach to patient careKey Attributes:• Dedication, patience, and professionalism• Team-oriented with willingness to learn and adaptAbout the Company:Apollo Clinic, Beliaghata, is part of India’s trusted Apollo Healthcare network, committed to delivering high-quality medical services and patient-centered care. The clinic focuses on modern treatment methods, preventive healthcare, and professional development for its staff.
Role & Responsibilities • Provide medical leadership and oversight for medical safety and medical monitoring activities across assigned programs. • Ensure compliance with applicable federal, local, and international regulations and guidelines related to clinical research, safety, and Good Clinical Practice (GCP). • Review, assess, and interpret safety data from clinical trials and post-marketing sources. • Provide expert medical consultation and advice across multiple projects and assignments. • Establish priorities, manage deadlines, and ensure timely delivery of safety-related objectives. • Collaborate effectively with internal teams, senior management, and external clients. • Demonstrate leadership in project planning, execution, and financial management where applicable. • Support strategic decision-making related to safety risk assessment and benefit-risk evaluation. Qualifications • Medical degree from an accredited and internationally recognized medical school with curriculum relevant to general medical education. • Valid medical license or equivalent from the country or region of practice. • Strong understanding of clinical research, pharmaceutical development, and safety regulations. Experience • Minimum 5 years of clinical practice experience after award of medical degree, or equivalent combination of education, training, and experience. • Graduate medical training may be considered toward clinical practice experience. • Alternatively, 3 years of clinical practice experience with an additional 2 years as a pharmaceutical physician in any role. • Minimum 5 years of medical safety or medical monitoring experience in the pharmaceutical or related industry. Skills • Strong knowledge of clinical trial processes, pharmaceutical research, and safety regulations. • Excellent ability to manage priorities, objectives, and timelines effectively. • Strong consultation, advisory, and decision-making skills across multiple assignments. • Proven leadership skills with aptitude for project and financial management. • Ability to build and maintain effective working relationships with coworkers, managers, and clients. • Excellent written and verbal communication skills in English. About the Company • IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, IQVIA creates intelligent connections to accelerate the development and commercialization of innovative medical treatments.
Roles & Responsibilities • Perform medical device complaint investigations in compliance with global regulatory standards • Conduct risk assessments and support product safety evaluations • Analyze device-related adverse events and technical complaints • Prepare, review, and maintain investigation reports with high documentation accuracy • Collaborate with cross-functional global teams for complaint resolution and root cause analysis • Ensure adherence to medical device regulations, quality systems, and SOPs Qualification • B.Pharm / M.Pharm • Biomedical Engineering / Mechanical Engineering • B.Sc Medical Imaging & Radiology Technology • Master’s in Molecular Biology • B.Sc Nursing • BDS (Bachelor of Dental Surgery) Experience • 0-5 years of experience in medical device investigation, complaint handling, or related safety/quality roles • Prior exposure to medical device safety processes preferred Skills • Strong knowledge of medical devices, complaint investigation, and risk assessment • Excellent verbal and written English communication skills • Good analytical, documentation, and problem-solving abilities • Willingness to work in rotational and night shifts • Ability to collaborate with global stakeholders Walk-In Details • Dates: 15th & 16th January 2026 • Reporting Time: 10:00 AM – 12:00 PM • Venue: Gate 1, Plot No. 8 & 9, Block DM, Sector V, Salt Lake, Kolkata, West Bengal – 700091 • Documents Required: Updated resume (CV) and original government ID proof About the Company Wipro is a global leader in IT, consulting, and healthcare & life sciences services, delivering end-to-end solutions across pharmacovigilance, medical devices, clinical research, and regulatory domains, with a strong focus on quality, compliance, and innovation.
Role & Responsibilities • Execute medical affairs strategy for the assigned geographic zone • Understand disease trends, treatment practices and therapeutic needs through KOL engagement, scientific meetings and journal reviews • Disseminate credible, non-promotional scientific information to internal and external stakeholders • Execute medical projects including IIS (Investigator Initiated Studies) • Support medico-marketing strategies and provide regular field insights to management • Identify and develop relationships with Key Opinion Leaders and Expert Experts (EEs) • Support registration of new products and indications by providing medical rationale, literature support and scientific presentations • Support defence of marketed products with regulators, NGOs and media as required • Write, review and revise labeling and scientific documentation as per SOPs • Support regulatory affairs activities and stakeholder engagement Qualifications • Medical degree (MD preferred, Pharmacology specialization preferred) or life sciences qualification Experience• 0–3 years of experience in Medical Affairs / Pharmaceutical / Healthcare industry (fresh MD Pharmacology graduates can apply) • Candidates without doctoral qualification require 10+ years of relevant field-based scientific experience • Strong scientific knowledge of Diabetes therapy area • Good interpersonal and communication skills Skills • Scientific communication and presentation skills • KOL relationship management • Medical writing and documentation skills • Analytical and field-insight generation ability • Basic IT proficiency (MS Office) • Ability to work independently in field medical roles About the Company • Boehringer Ingelheim is a global biopharmaceutical company active in human and animal health
Role & Responsibilities • Perform and interpret diagnostic imaging procedures including X-ray, CT Scan, MRI and Ultrasound • Review and report imaging findings accurately within defined turnaround time • Provide E-reporting support for PPP units (MRI & CT Scan) • Consult with referring physicians regarding imaging results and recommendations • Ensure strict adherence to radiation safety and hospital compliance protocols • Maintain accurate imaging records and patient documentation • Participate in multidisciplinary case discussions for patient care Qualifications & Experience • DMRD / DNB Radiology / DMRE / DM Radiology / DRIT • 1–2 years of post-qualification radiology experience • Strong diagnostic interpretation and reporting abilities • Good communication and clinical coordination skills Skills • Diagnostic imaging and reporting proficiency • Analytical and problem-solving skills • High attention to detail and report accuracy • Patient interaction and clinical coordination • Time management and efficiency in report delivery About the Company • Eskag Sanjeevani Pvt Ltd is a healthcare services organisation providing diagnostic and clinical services across PPP healthcare units, focused on delivering accessible and high-quality radiology services
Roles & Responsibilities • Perform medical device complaint investigations in compliance with ISO 13485 and ISO 14971 • Conduct risk assessments, hazard analysis, and FMEA • Support CAPA initiation, investigation, and closure activities • Prepare, review, and maintain high-quality investigation and compliance documentation • Ensure adherence to global regulatory and quality system requirements • Collaborate with cross-functional and global teams for complaint resolution • Support audit readiness and continuous quality improvement initiatives Qualifications • Any Life Science Graduate • For Kolkata location: B.Pharm / M.Pharm, Biomedical / Mechanical Engineering / B.Sc Medical Imaging & Radiology / M.Sc Molecular Biology / B.Sc Nursing / BDS Experience • Pune & Hyderabad: 3-9 years (Immediate joiners preferred) • Kolkata: 0-5 years (Relevant medical device investigation experience required) Skills • Medical Device Complaint Investigation • ISO 14971 Risk Management • ISO 13485 Quality Management Systems • CAPA, Root Cause Analysis • FMEA and Risk Assessment • Excellent English communication skills • Willingness to work rotational shifts and from office Walk-In Interview Details Hyderabad Dates: 12, 15 & 16 January 2026 Venue: Wipro Limited, Manikonda STPI, Tower 6, 3rd Floor, Gachibowli, Hyderabad – 500032 Contact: Pavan Pune Dates: 12, 14 & 16 January 2026 Venue: Unit 2, Plot No. 31, Hinjewadi Phase 2, Rajiv Gandhi Infotech Park, Pune – 411057 Contact: Riya / Varsha Kolkata Dates: 13, 15 & 16 January 2026 Venue: Gate 1, Plot 8 & 9, Block DM, Sector V, Salt Lake, Kolkata – 700091 Contact: Sarita Reporting Time: 10:00 AM – 12:30 PM Documents to Carry • Updated Resume • Original Government ID Proof • Mention source of walk-in information on top of CV About the Company Wipro Limited is a leading global information technology, consulting, and business services company with a strong presence in healthcare and medical devices. Wipro supports global clients with regulatory-compliant quality, safety, and post-market surveillance services, offering professionals exposure to international standards, advanced technologies, and long-term career growth opportunities.
Roles & Responsibilities: • Prepare summary reports for medical devices • Perform trend analysis on customer complaints and product performance • Conduct monthly and ad-hoc data analysis from complaints, sales, and trending databases • Carry out literature searches and review clinical, scientific, and medical references • Identify, interpret, and evaluate data from medical literature, clinical studies, and post-market sources • Compile and submit clinical and post-market surveillance (PMS) documents • Support international regulatory submissions in line with global medical device regulations • Contribute to PMS plans and safety reports for assigned device portfolios Qualification: • Relevant degree in Life Sciences, Biomedical Engineering, Pharmacy (B.Pharm, D.Pharm, M.Pharm) , or related discipline Experience: • 3-6 years of experience in Medical Devices domain • Hands-on experience in medical review and post-market surveillance Skills: • Strong knowledge of medical device regulations and PMS requirements • Experience in complaint trending and safety data analysis • Expertise in literature search and regulatory documentation • Excellent analytical, documentation, and communication skills • Ability to work in a fast-paced, office-based environment • Immediate joiners preferred About the Company: ANRI Solutions is a leading recruitment partner connecting skilled professionals with top pharmaceutical, medical device, and healthcare organizations across India and globally.
Role & Responsibilities: • Dispense medications accurately and provide clear instructions on proper usage and dosage • Conduct patient consultations to assess medication needs and offer personalized guidance • Develop and support medication therapy plans in collaboration with healthcare professionals • Work closely with the medical team to ensure effective patient care and medication adherence • Maintain accurate patient records including medication histories and treatment plans • Stay updated on new drugs, therapies, and best practices in pharmacy care Qualification: • Bachelor of Pharmacy (B.Pharm) or equivalent qualification from a recognized institution Experience: • Freshers or candidates with relevant hospital or clinical pharmacy experience are welcome About the Company: Fortis Healthcare is one of India’s leading integrated healthcare delivery providers, known for its clinical excellence, advanced medical infrastructure, and patient-centric services. With a strong presence across hospitals, diagnostic centers, and specialty clinics, Fortis Healthcare is committed to delivering high-quality care while offering a professional environment that supports learning, growth, and excellence in healthcare services.
Role & Responsibilities • Assist in processing Adverse Events (AE) and endpoint data, including intake, tracking, and workflow distribution • Track safety case timelines and ensure timely submissions to clients and stakeholders • Support Lifecycle Safety database entry, quality control, and report generation • Coordinate safety report submissions to regulatory authorities and investigators • Maintain project files, case folders, and document control systems • Assist with project start-up activities, system access, and administrative workflows • Archive safety data and manage records post-study closure • Support database validation, user testing, and ad-hoc data searches • Coordinate meetings, courier dispatch, and administrative logistics • Mentor junior administrative staff and support continuous process improvement Qualification • Degree in Life Sciences, Pharmacy, Healthcare, or an allied scientific discipline Experience • Minimum 1 year of relevant experience in pharmacovigilance, clinical research, or safety operations Skills • Good understanding of GCP, ICH guidelines, SOPs, and safety workflows • Working knowledge of medical terminology • Proficiency in Microsoft Office and web-based applications • Strong organizational, multitasking, and time-management skills • Excellent written and verbal communication skills • High attention to detail, accuracy, and compliance About the Company • IQVIA is a globally recognized leader in clinical research, pharmacovigilance, and healthcare intelligence, supporting life sciences companies in the development and commercialization of innovative medical treatments.