Associate Pharmacovigilance Specialist Vacancies at Clarivate
- Clarivate Hiring Associate Pharmacovigilance Specialist | Drug Safety Jobs in Karnataka
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Preferred Technical Skills
- Eligibility / Qualifications
- Educational Qualification
- Experience Required
- Essential Skills
- Location & Salary
- Job Location
- Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What is the role offered by Clarivate?
- 2. What qualifications are eligible for this pharmacovigilance job?
- 3. How much experience is required for this role?
- 4. What skills are important for this position?
- 5. Is this a remote or hybrid role?
- 6. What is the expected salary for this role?
- Summary Table
Clarivate Hiring Associate Pharmacovigilance Specialist | Drug Safety Jobs in Karnataka
Pharmacovigilance professionals looking for drug safety and biomedical literature review jobs in India now have an excellent opportunity with Clarivate. The company is currently hiring Associate Pharmacovigilance Specialists for its Life Sciences and Healthcare division in Karnataka. This hybrid work opportunity is ideal for candidates with experience in adverse event reporting, biomedical literature monitoring, drug safety operations, medical writing, and pharmacovigilance compliance.
As pharmaceutical and biotechnology companies continue strengthening global drug safety surveillance, regulatory compliance systems, and patient safety monitoring programs, the demand for pharmacovigilance professionals with biomedical literature expertise is rapidly increasing across India. Clarivate is expanding its pharmacovigilance and healthcare analytics operations and actively seeking professionals who can support literature monitoring, ICSR assessments, medical summaries, safety indexing, and healthcare compliance documentation.
Candidates with prior experience in biomedical literature review, adverse event reporting, medical writing, healthcare documentation, and pharmacovigilance services will find this opportunity highly valuable for long-term career growth in the pharmaceutical and healthcare industry.
Company Overview
Clarivate is a globally recognized information services and healthcare analytics company providing advanced solutions across life sciences, healthcare, intellectual property, regulatory compliance, and scientific research sectors.
The organization supports pharmaceutical, biotechnology, and healthcare companies through scientific intelligence, biomedical literature services, pharmacovigilance operations, and healthcare data management solutions. Clarivate plays a major role in helping healthcare organizations improve drug safety monitoring, regulatory submissions, patient safety systems, and scientific research analysis.
The company’s Life Sciences and Healthcare division works extensively on pharmacovigilance operations, biomedical literature surveillance, healthcare compliance management, and medical content analysis. Employees gain exposure to global pharmaceutical clients, regulatory standards, advanced healthcare technologies, and scientific information systems.
Clarivate also promotes employee learning, career development, and flexible work culture while offering opportunities to work on international healthcare and drug safety projects.
Job Role & Responsibilities
Clarivate is hiring candidates for the role of Associate Pharmacovigilance Specialist to support biomedical literature monitoring, adverse event identification, ICSR analysis, and healthcare safety documentation activities.
This pharmacovigilance role requires strong analytical skills, biomedical terminology knowledge, scientific writing abilities, and understanding of global drug safety regulations.
Key Responsibilities
- Analyse biomedical literature and internal drug safety alerts for adverse event reporting
- Identify Individual Case Safety Reports (ICSRs) and safety-relevant information impacting product safety profiles
- Prepare brief narratives summarizing ICSR criteria and safety-related information
- Review biomedical literature batches according to regulatory timelines and quality standards
- Use drug safety systems to maintain audit-ready tracking and assessment history
- Select relevant articles for inclusion in client product literature databases
- Create detailed and accurate article abstracts using proper scientific writing practices
- Extract key scientific information and develop comprehensive indexing for literature retrieval
- Ensure timely completion of indexing and abstracting activities according to regulatory submission timelines
- Maintain awareness of new drugs, therapeutic categories, disease entities, and biomedical terminology updates
- Support terminology maintenance and literature search activities according to business requirements
- Demonstrate understanding of client drug labels and apply safety assessment knowledge effectively
Preferred Technical Skills
Candidates applying for this pharmacovigilance and drug safety role should have practical knowledge in:
- Pharmacovigilance operations
- Adverse event reporting
- Biomedical literature monitoring
- ICSR assessment
- Drug safety surveillance
- Medical writing
- Regulatory compliance
- Healthcare documentation
- Scientific abstract writing
- Biomedical indexing
- Safety database systems
- Clinical safety reporting
- Pharmaceutical risk management
- Healthcare analytics
- Scientific literature review
Candidates with prior exposure to CRO operations, pharmaceutical safety systems, healthcare consulting, and medical information services will have an added advantage.
Eligibility / Qualifications
Candidates interested in this Associate Pharmacovigilance Specialist vacancy should meet the following eligibility criteria.
Educational Qualification
Applicants should possess a Master’s Degree in Life Sciences, Healthcare, or Biomedical Sciences.
Eligible educational qualifications include:
M.Pharm, B.Pharm, Pharm.D, MSc, Biotechnology, Microbiology, Biochemistry, Biophysics, Biomedical Sciences, Clinical Research, Life Sciences, Pharmaceutical Sciences, Nursing, Dentistry, Physiotherapy, Healthcare Management, Medical Laboratory Sciences, or related healthcare and life science disciplines.
Experience Required
- Minimum 1–2 years of experience reviewing biomedical literature for adverse event reporting
- Prior experience in pharmacovigilance or drug safety operations preferred
- Experience in medical writing, scientific summaries, or healthcare documentation beneficial
- Working knowledge of biomedical terminology and therapeutic areas required
Essential Skills
- Strong analytical and scientific interpretation skills
- Ability to summarize biomedical literature accurately
- Excellent English communication and writing skills
- Knowledge of pharmacovigilance regulations and drug safety systems
- Understanding of biomedical terminology and therapeutic areas
- Good grammar, organization, and scientific writing abilities
- Flexibility and adaptability to changing client requirements
- Strong time management and attention to detail
Location & Salary
Job Location
Karnataka
Salary
Based on current market trends and pharmacovigilance industry standards in India, the expected salary for the Associate Pharmacovigilance Specialist role may range approximately between ₹4.5 LPA to ₹7.5 LPA depending on candidate experience, biomedical literature expertise, and interview performance.
Application Process
Interested and eligible candidates can apply online through the official Clarivate careers portal.
Apply Here: https://careers.clarivate.com/job/CLACLAGBJREQ135672EXTERNALENGB/Associate-Pharmacovigilance-Specialist
Candidates should keep their updated resume, pharmacovigilance experience details, biomedical literature review exposure, and scientific writing samples ready before applying.
Early applications are recommended because hiring demand for drug safety and pharmacovigilance professionals remains high across India’s pharmaceutical and healthcare sectors.
Frequently Asked Questions (FAQs)
1. What is the role offered by Clarivate?
Clarivate is hiring candidates for the position of Associate Pharmacovigilance Specialist in Karnataka.
2. What qualifications are eligible for this pharmacovigilance job?
Candidates with M.Pharm, B.Pharm, Pharm.D, MSc, Biotechnology, Microbiology, Biochemistry, Nursing, Dentistry, Physiotherapy, and related life sciences qualifications can apply.
3. How much experience is required for this role?
Applicants should have at least 1–2 years of experience in biomedical literature review, adverse event reporting, or pharmacovigilance operations.
4. What skills are important for this position?
Biomedical literature monitoring, ICSR assessment, medical writing, adverse event reporting, scientific documentation, and pharmacovigilance compliance skills are important for this role.
5. Is this a remote or hybrid role?
This position follows a hybrid work model.
6. What is the expected salary for this role?
The expected salary may range approximately between ₹4.5 LPA to ₹7.5 LPA depending on candidate experience and technical expertise.
Summary Table
| Category | Details |
|---|---|
| Company | Clarivate |
| Department Vacancies | Associate Pharmacovigilance Specialist, Life Sciences & Healthcare |
| Qualification | M.Pharm, B.Pharm, Pharm.D, MSc, Biotechnology, Microbiology, Biochemistry, Nursing, Dentistry, Physiotherapy |
| Experience | 1–2 Years |
| Location | Karnataka |
To apply for this job please visit careers.clarivate.com.
