Unlock pharmacovigilance jobs in India with Clarivate’s hybrid role. Ideal for freshers in pharmaceutical careers, focusing on adverse event reporting and literature screening. Apply now for drug safety opportunities!
About the Company
Clarivate is a global analytics leader empowering innovation across life sciences and healthcare, with decades of expertise in data-driven insights. Renowned for its credibility in supporting regulatory compliance and accelerating breakthroughs, Clarivate serves thousands of organizations worldwide through advanced platforms like Cortellis and Derwent.
The company’s innovative solutions drive growth in pharmacovigilance, clinical trials, and market intelligence, ensuring seamless global presence in over 100 countries. Committed to ethical standards and diversity, Clarivate fosters a collaborative environment where professionals thrive in a rapidly evolving pharma landscape, contributing to safer therapies and better patient outcomes.
Job Details
- Company Name: Clarivate
- Experience: Fresher / Up to 2 years in biomedical literature review for adverse events
- Qualification: Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
- Location: Available in 2 locations (India-based)
- Work Type: Hybrid / Regular hours 12:00 PM to 9:00 PM
Job Description
Clarivate is hiring for its Pharmacovigilance team to bolster drug safety monitoring in the life sciences sector. This entry-level role supports critical adverse event reporting through literature analysis, ensuring compliance with global regulations. Join a dynamic group blending market research and healthcare consulting expertise.
Associate Pharmacovigilance Specialist
- Department: Life Sciences & Healthcare
- Market: Global pharmaceutical and healthcare sectors
- Role: Screen biomedical literature for safety signals and adverse events
- Experience: Fresher / Up to 2 years
- Education/Qualification: Master’s Degree in relevant sciences
Skills/Qualifications
- Strong analytic ability to summarize biomedical case reports and studies
- Working knowledge of biomedical terminology, drugs, and therapeutic areas
- Experience with commercial and client-specific literature databases
- Related background in drug safety or pharmacovigilance desirable
- Proficiency in scientific/medical writing (advantageous)
- Certification from a professional medical writer’s association (preferred)
- Degree in Dentistry, Physiotherapy, or Nursing for patient exposure (bonus)
Key Responsibilities
- Screen biomedical literature for pharmaceutical safety information
- Assess adverse events for regulatory reporting compliance
- Conduct regular reviews to capture potential safety signals
- Identify and report relevant adverse event cases accurately
- Analyze literature using medical terminology and drug knowledge
Benefits/Perks
- Career growth in pharmacovigilance and drug safety leadership
- Learning opportunities through global training and certifications
- Competitive salary aligned with pharma industry standards
- Collaborative work culture emphasizing innovation and teamwork
- Global exposure to diverse healthcare projects and markets
How to Apply
To apply for the Associate Pharmacovigilance Specialist position, visit Clarivate’s careers portal at https://clarivate.wd5.myworkdayjobs.com/careers, search for Job ID JREQ134094, and submit your resume, cover letter, and qualifications online. Highlight your biomedical literature experience for faster review.
Verified Pharmacovigilance Job
The post is released by the Clarivate Career page. Click here to visit the post
For tailored pharma jobs in India and expert guidance, check Pharma Recruiter. Seize this drug safety opportunity—apply today and advance your pharmaceutical career!
Why You Should Join
Clarivate cultivates an inclusive company culture celebrated for equal opportunities, professional development, and recognition of diverse talents, creating a supportive space where freshers quickly integrate into impactful roles.
With unwavering long-term career stability fueled by the company’s expansion in life sciences analytics, you’ll enjoy secure progression amid industry shifts. Dive into rich learning and growth opportunities, from hands-on pharmacovigilance training to cross-functional collaborations on cutting-edge projects.
In a compliance-centric environment blending regulatory rigor with innovative tools, you’ll pioneer safer drug monitoring while contributing to global health advancements that truly matter.
FAQs
What eligibility is required for Clarivate’s pharmacovigilance jobs?
A Master’s in Life Sciences or related fields is essential, with fresher status or up to 2 years in literature review for adverse events. Drug safety experience boosts your profile for these pharma jobs in India.
How does the application process work for this hybrid role?
Search Job ID JREQ134094 on Clarivate’s careers site, upload your documents, and apply directly. Interviews follow shortlisting, focusing on analytic skills and biomedical knowledge.
Are there growth opportunities in drug safety at Clarivate?
Yes, roles evolve into senior pharmacovigilance positions with training, certifications, and global exposure, supporting long-term pharmaceutical careers in healthcare consulting.
What salary can I expect for entry-level QA jobs like this?
Salaries are competitive for freshers, varying by experience; full details shared post-interview. Perks include hybrid flexibility and professional development for comprehensive rewards.
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