Apply for Clarivate Hiring for Associate Pharmacovigilance Specialist. Exciting opportunity in drug safety, literature monitoring, and pharmacovigilance services.
About the Role
Clarivate, a global leader in data-driven insights and analytics, is hiring an Associate Pharmacovigilance Specialist to join its Life Sciences and Healthcare division. This is a unique opportunity for life science professionals passionate about drug safety, biomedical research, and patient health to contribute to the monitoring and evaluation of adverse events through scientific literature. Clarivate Hiring for Associate Pharmacovigilance Specialist
As an Associate Pharmacovigilance Specialist, you will play a critical role in ensuring that medical and pharmaceutical products are monitored for safety and compliance with global pharmacovigilance regulations. You will be responsible for biomedical literature screening, data analysis, indexing, and summarizing case reports with accuracy and scientific precision. Clarivate Hiring for Associate Pharmacovigilance Specialist
This position is ideal for individuals who have a keen eye for detail, excellent analytical and writing skills, and a strong understanding of medical terminology and pharmacovigilance processes.
Key Responsibilities
As part of the Pharmacovigilance team at Clarivate, your day-to-day responsibilities will include: Clarivate Hiring for Associate Pharmacovigilance Specialist
- Biomedical Literature Monitoring:
Conduct detailed reviews of global biomedical literature to identify adverse events and safety signals related to drugs, vaccines, or medical devices. - Adverse Event Assessment:
Assess identified case reports to determine the seriousness, expectedness, and relevance of adverse events according to international pharmacovigilance guidelines. - Indexing and Abstracting:
Summarize complex biomedical case reports and studies into concise and scientifically accurate abstracts for internal and regulatory reporting. - Compliance and Reporting:
Ensure adherence to ICH-GCP, global pharmacovigilance regulations, and client-specific reporting requirements. Maintain high-quality standards in all deliverables. - Collaboration and Communication:
Work closely with global safety teams, project managers, and scientific experts to meet timelines and ensure accurate information flow. - Database Management:
Use commercial and client-specific literature databases to track, record, and manage case information effectively. - Quality Documentation:
Maintain meticulous documentation of case assessments, literature searches, and reports in compliance with SOPs and data protection regulations. - Process Improvement:
Contribute to refining pharmacovigilance workflows, enhancing efficiency, and ensuring continuous process improvement. - Clarivate Hiring for Associate Pharmacovigilance Specialist
About You – Education, Experience, and Skills
To succeed in this role, you must bring a strong combination of scientific expertise, analytical capability, and attention to detail. Clarivate Hiring for Associate Pharmacovigilance Specialist
Educational Qualifications
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences such as Pharmacy, Microbiology, Biochemistry, Biotechnology, or Biophysics.
- Candidates with degrees in Dentistry, Physiotherapy, or Nursing with hospital-based patient exposure will have an added advantage.
- Alternatively, a degree in Information Science with experience in drug and patient safety can also be considered.
Experience Requirements
- 1 to 2 years of experience in reviewing biomedical literature for adverse event reporting or equivalent roles.
- Related experience in pharmacovigilance, drug safety, or medical writing will be an asset.
- Hands-on familiarity with biomedical literature databases such as PubMed, Embase, or client-specific tools.
Technical & Professional Skills
- Strong analytical and critical-thinking skills to assess and summarize biomedical data accurately.
- Excellent English communication skills — verbal, written, and comprehension.
- Ability to prepare concise, accurate, and scientifically sound summaries.
- Working knowledge of pharmacovigilance regulations, ICH-GCP guidelines, and drug safety reporting requirements.
- Strong command of medical and scientific terminology, therapeutic areas, and drug classifications.
- Basic computer literacy, including proficiency in MS Office applications.
- Experience with MedDRA coding, case processing, or Argus Safety database is desirable.
- Clarivate Hiring for Associate Pharmacovigilance Specialist
Soft Skills
- High attention to detail with a commitment to quality and compliance.
- Ability to work effectively both independently and collaboratively within a global team.
- Adaptability to dynamic client needs and a fast-paced environment.
- Strong organizational and time management skills to handle multiple projects.
- Clarivate Hiring for Associate Pharmacovigilance Specialist
Preferred Qualifications
While not mandatory, the following will be an added advantage:
- Certification from a professional medical writers association.
- Background in scientific or medical writing.
- Prior experience in drug safety surveillance or pharmaceutical regulatory affairs.
Work Environment and Schedule
- Work Hours: Monday to Friday
- Mode of Work: Hybrid
- Location: Noida, Bengaluru
- Employment Type: Full-Time, Permanent
This hybrid model allows a balance between remote flexibility and on-site collaboration, providing the ideal work-life balance for professionals in life sciences.
About Clarivate
Clarivate™ is a leading global provider of transformative intelligence that connects data, analytics, and deep domain expertise to drive innovation and growth.
With operations across Academia & Government, Intellectual Property, and Life Sciences & Healthcare, Clarivate empowers organizations to accelerate research, protect ideas, and improve patient outcomes.
In the Life Sciences and Healthcare division, Clarivate offers comprehensive pharmacovigilance, regulatory, and clinical research services that help pharmaceutical companies ensure product safety and compliance.
Clarivate Hiring for Associate Pharmacovigilance Specialist
Our Values:
- Innovation: We continuously enhance our data-driven solutions to improve healthcare intelligence.
- Integrity: We uphold the highest ethical standards in pharmacovigilance and scientific reporting.
- Collaboration: We foster a culture where teamwork and communication drive collective success.
- Diversity and Inclusion: We value diverse perspectives that contribute to creativity and innovation.
Clarivate’s commitment to data quality and transparency makes it a trusted partner for global pharmaceutical companies, regulatory authorities, and healthcare organizations. Clarivate Hiring for Associate Pharmacovigilance Specialist
Why Join Clarivate?
Working at Clarivate means joining a global network of talented professionals who share a common mission — to advance research, enhance drug safety, and improve patient lives.
Here’s what makes Clarivate an employer of choice in the life sciences industry:
- Global Exposure: Collaborate with international clients, regulatory bodies, and scientific experts.
- Continuous Learning: Access structured training, certifications, and learning programs to enhance your pharmacovigilance skills.
- Career Growth: Progress through a clearly defined career path in drug safety, regulatory affairs, or medical writing.
- Innovation Culture: Be part of a company that integrates cutting-edge technology and scientific insights.
- Employee Well-being: Enjoy hybrid work flexibility, health benefits, and an inclusive work environment.
If you are a detail-oriented professional who is passionate about pharmacovigilance and committed to patient safety, this is an excellent opportunity to grow your career with a leading global organization.
Role Overview
- Job Title: Associate Pharmacovigilance Specialist
- Department: Healthcare & Life Sciences
- Role Category: Other Hospital Staff
- Industry Type: IT Services & Consulting
- Employment Type: Full Time, Permanent
- Location: Noida, Bengaluru
- Company Name: Clarivate
Key Skills
Pharmacovigilance, Drug Safety, Medical Writing, Biomedical Research, Clinical Trials, Adverse Event Reporting, MedDRA Coding, Case Processing, ICH-GCP Guidelines, Patient Safety, Literature Screening, Life Sciences, Regulatory Affairs, Clinical Data Management, Argus Safety, Pharmacology, Clarivate Hiring for Associate Pharmacovigilance Specialist
How to Apply
Interested candidates who meet the eligibility criteria can apply online by visiting the official Clarivate Careers page.
Steps to Apply:
- Visit the official website: https://clarivate.com/careers
- Search for “Associate Pharmacovigilance Specialist” in the Careers section.
- Review the job details carefully to ensure you meet the qualifications.
- Click “Apply Now” and complete the online application form.
- Upload your updated resume and cover letter highlighting relevant experience.
- Submit your application and wait for confirmation from the Clarivate HR team.
Alternatively, candidates can stay updated through professional job portals or follow Clarivate’s official LinkedIn page for new opportunities in pharmacovigilance and life sciences. Clarivate Hiring for Associate Pharmacovigilance Specialist
Final Thoughts
The Associate Pharmacovigilance Specialist position at Clarivate is an excellent opportunity for professionals looking to advance in the field of pharmacovigilance, drug safety, and medical writing. With global exposure, a collaborative culture, and a mission-driven environment, Clarivate provides an ideal platform to contribute to global patient safety and medical research excellence. Clarivate Hiring for Associate Pharmacovigilance Specialist
Start your journey today and be part of a team that is transforming life sciences through innovation and intelligence.
Apply now and take your career to the next level with Clarivate!
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
