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Clarivate
Associate Pharmacovigilance Specialist | Clarivate | Hybrid India
Clarivate hiring Associate Pharmacovigilance Specialist (Hybrid India). Master’s in Life Sciences with 1–2 years PV experience required.
Clarivate, a global leader in healthcare, life sciences, and data intelligence solutions, is inviting applications for the position of Associate Pharmacovigilance Specialist. This role is available in hybrid mode across India, offering professionals the chance to work in drug safety, biomedical literature monitoring, and pharmacovigilance reporting.
Company Overview
Clarivate is recognized worldwide for delivering trusted data, insights, and analytics to accelerate innovation in healthcare, life sciences, and beyond. With expertise in drug safety monitoring, regulatory intelligence, and medical writing, Clarivate supports pharma and biotech companies in achieving compliance and improving patient outcomes. By joining Clarivate, candidates become part of an organization committed to advancing global healthcare systems through innovation and scientific expertise.
Job Role & Responsibilities
As an Associate Pharmacovigilance Specialist, you will:
- Perform biomedical literature monitoring for adverse event reporting.
- Assess, index, and abstract biomedical literature using in-depth knowledge of medical and scientific terminology.
- Review case reports, studies, and publications for drug safety signals.
- Summarize biomedical data into accurate and concise safety reports.
- Support regulatory compliance in pharmacovigilance and drug safety operations.
- Collaborate with cross-functional teams to ensure high-quality deliverables.
- Adapt to changing client needs and maintain flexibility in workload.
Eligibility / Qualifications
- Education:
- Master’s in Life Sciences, Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Biomedical Sciences, or Health Sciences.
- Degree in Dentistry, Physiotherapy, or Nursing (with hospital-based patient exposure) is an added advantage.
- Experience:
- 1–2 years of experience reviewing biomedical literature for adverse events OR equivalent education/experience in drug safety.
- Prior exposure to pharmacovigilance, drug safety, or medical writing desirable.
- Skills:
- Strong analytical ability for summarizing biomedical reports.
- Knowledge of drugs, therapeutic areas, and pharmacovigilance regulations.
- Excellent English (written and spoken).
- Experience with biomedical databases (commercial or client-specific).
- Proficiency in medical/scientific writing.
Desirable:
- Certification in medical writing (preferred).
- Experience with pharmacovigilance literature databases.
Location & Salary
- Work Mode: Hybrid (India)
- Work Hours: Monday to Friday
- Compensation: Competitive salary + global benefits aligned with Clarivate’s policies.
- Employment Type: Full-time
Application Process
Interested candidates can apply online through Clarivate’s official career portal:
👉 Apply Here
FAQs
1. What is the role of an Associate Pharmacovigilance Specialist?
Monitoring biomedical literature for adverse event reporting, summarizing data, and supporting drug safety compliance.
2. What qualifications are required?
A Master’s in Life Sciences or related fields, with 1–2 years of PV/drug safety experience.
3. Is this role suitable for freshers?
No. At least 1 year of relevant experience is required.
4. What is the work mode?
The role is hybrid, offering flexibility to work both remotely and from the office.
5. What skills are most important?
Analytical ability, biomedical terminology knowledge, medical writing, and database expertise.
Quick Summary Table
| Company | Clarivate |
|---|---|
| Vacancy | Associate Pharmacovigilance Specialist |
| Location | Hybrid (India) |
| Required Education | Master’s in Life Sciences, Pharmacy, Biochemistry, Microbiology, Biotechnology, Biophysics, Biomedical Sciences, Dentistry, Physiotherapy, Nursing |
| Experience | 1–2 years PV/drug safety/literature review |
| Skills | Biomedical databases, medical writing, pharmacovigilance regulations |
| Employment Type | Full-time (Hybrid) |
| Salary | Competitive with global benefits |
| Apply Link | Clarivate Careers Portal |
To apply for this job please visit careers.clarivate.com.