Clarivate Hiring Freshers For Associate Pharmacovigilance Specialist: Apply Now
Clarivate is inviting applications for the role of Associate Pharmacovigilance Specialist at its Noida, Uttar Pradesh office, offering a flexible hybrid working model. This position is open to candidates holding a Master’s degree in Life Sciences and up to 2 years of experience in pharmacovigilance or biomedical literature review.
This opportunity is particularly well‑suited for freshers and early‑career professionals who want to build a strong foundation in the pharmacovigilance domain. The role provides exposure to key drug safety activities such as ICSR processing, biomedical literature surveillance, and safety data evaluation, making it an excellent entry point for those aiming to grow in PV roles within India.
Job Overview
- Position: Associate Pharmacovigilance Specialist
- Department: PV
- Location: Noida, Uttar Pradesh, India (Hybrid – 2–3 days/week office)
- Experience: 0 to 2 Years
- Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, Lifesciences, Nursing , Clinical Research
- Job Type: Full-Time
- Application Deadline: 27 Feb 2026
About the Hiring Organization
Clarivate is a leading global provider of transformative intelligence, delivering advanced data, analytics, and workflow solutions that help organizations across the world accelerate innovation. The company supports key sectors such as academia, government, intellectual property, and life sciences, enabling professionals to make smarter, evidence‑based decisions.
With operations spanning over 180 countries and a global workforce of approximately 12,000 employees, Clarivate plays a critical role in powering scientific discovery, healthcare advancement, and regulatory compliance. It is headquartered in London, United Kingdom, with additional operational centers in the United States and other international locations.
Key Responsibilities
- Critically review biomedical literature:
Evaluate large volumes of published biomedical articles and internal drug safety alerts to identify Individual Case Safety Reports (ICSRs) and other safety‑relevant findings that may influence the risk–benefit or safety profile of the client’s products. All assessments must follow applicable regulatory guidelines and standard operating procedures. - Summarize safety findings:
Prepare clear and concise narratives highlighting ICSR criteria and any additional safety‑relevant insights identified in each article. - Apply product knowledge:
Demonstrate a solid understanding of the client’s drug labels, indications, and safety information, using this knowledge effectively during safety assessments. - Ensure timely and accurate reviews:
Complete the evaluation of each assigned biomedical literature batch accurately, thoroughly, and within required timelines, maintaining compliance with client quality expectations. - Maintain complete documentation:
Use the designated drug safety system to document all actions, assessments, and decisions, ensuring the creation of an audit‑ready, traceable reference history.
Required Skills & Qualifications
We are looking for motivated professionals who can contribute to clinical compliance and operational excellence. The ideal candidate should have the following qualifications:
- Educational Background:
- Master’s degree in Life Sciences, Health Sciences, or Biomedical Sciences, including disciplines such as Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related fields.
- Experience Level:
- Freshers or candidates with up to 2 years of experience in reviewing biomedical literature for adverse event reporting.
- OR
- An equivalent combination of education and experience—for example, a degree in Information Science with at least 1 year of relevant exposure to drug safety or patient safety support.
- Analytical Skills:
- Strong ability to analyze and summarize key findings from biomedical case reports, clinical studies, or topic‑specific scientific articles.
- Scientific Knowledge:
- Working understanding of biomedical terminology, drug classes, therapeutic areas, and the fundamentals of pharmacovigilance.
- Tool & Database Expertise:
- Exposure to commercial biomedical literature databases and client‑specific literature monitoring platforms used for identifying adverse events and safety signals.
Preferred Skills & Experience (Good to Have)
Candidates with the following additional skills and experience will have an advantage:
- Strong Time‑Management:Ability to manage tasks efficiently, prioritize workload, and meet tight deadlines while handling multiple literature batches.
- Excellent Communication Skills: Clear and professional written and verbal communication in English, essential for summarizing scientific content and interacting with global teams.
- High Motivation & Work Ethic: Demonstrates enthusiasm, accountability, and a proactive approach, thriving in a fast‑paced, deadline‑driven environment.
- Process Discipline: Consistent adherence to Standard Operating Procedures (SOPs), policies, and quality guidelines, ensuring accuracy and audit readiness.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
