Clarivate is inviting applications for the position of Associate/Pharmacovigilance Specialist at its Bangalore office. This hybrid opportunity is ideal for professionals with 2+ years of pharmacovigilance experience who have expertise in literature screening, scientific database searches, medical literature review, and drug safety surveillance.
If you are looking for Pharmacovigilance jobs in Bangalore, drug safety jobs in India, or literature screening jobs, this opportunity offers an excellent platform to work with a global healthcare intelligence company while contributing to patient safety and regulatory compliance.
Job Details
- Company: Clarivate
- Job Title: Associate/Pharmacovigilance Specialist
- Location: Bangalore, Karnataka, India
- Work Mode: Hybrid
- Job Type: Full-Time
- Experience: Minimum 2 Years
- Qualification: Bachelor’s Degree in Pharmacy, Life Sciences, Nursing, or related discipline
- Application Deadline: 23 July 2026
Key Responsibilities
As an Associate/Pharmacovigilance Specialist, you will:
- Perform structured searches in scientific databases including PubMed, Embase, and other medical literature databases.
- Execute literature screening using predefined search strategies.
- Identify adverse drug reactions, safety signals, and emerging safety risks.
- Conduct secondary review and evaluation of screened literature.
- Prepare accurate and medically sound abstracts for selected publications.
- Index scientific articles following internal pharmacovigilance standards.
- Apply medical judgment while summarizing scientific literature.
- Collaborate with Managers and Senior Managers to meet project timelines.
- Maintain high-quality documentation while ensuring regulatory compliance.
Required Qualifications
Candidates should possess:
- Bachelor’s degree in Pharmacy, Life Sciences, Nursing, or related healthcare discipline.
- Minimum 2 years of relevant Pharmacovigilance experience.
- Strong understanding of medical literature databases including:
- PubMed
- Embase
- Knowledge of literature screening methodologies.
- Excellent medical writing and scientific abstracting skills.
- Strong analytical and communication abilities.
- Ability to work collaboratively in global teams.
Preferred Skills
- Pharmacovigilance Literature Screening
- Drug Safety
- Medical Literature Review
- Signal Detection
- Adverse Event Identification
- Medical Writing
- Scientific Abstracting
- Regulatory Compliance
- Pharmacovigilance Operations
- Literature Surveillance
Why Join Clarivate?
Working with Clarivate provides professionals an opportunity to:
- Build expertise in global pharmacovigilance operations.
- Work with international pharmaceutical clients.
- Gain exposure to advanced literature surveillance processes.
- Develop medical writing and scientific evaluation skills.
- Enjoy a hybrid work environment.
- Work within a collaborative global healthcare team.
How to Apply
