MSc Life Science Jobs at Clarivate | Candidates Apply Now
Are you looking for MSc Life Science Jobs in the pharmacovigilance and drug safety sector? Clarivate is hiring for the role of Associate Pharmacovigilance Specialist in Karnataka, India. This is an excellent opportunity for candidates seeking Clarivate Careers and Biochemistry Jobs with experience in biomedical literature review, drug safety, and pharmacovigilance. Candidates from Life Sciences, Biotechnology, Microbiology, Pharmacy, and Biochemistry backgrounds can apply for this hybrid opportunity.
About the Company
Clarivate Official Website is a global leader in providing trusted insights and analytics to accelerate innovation in healthcare, life sciences, academia, and intellectual property. Through advanced scientific and biomedical data solutions, Clarivate supports organizations worldwide in research, drug safety, and healthcare innovation. The company offers excellent growth opportunities for professionals looking for Clarivate Careers, especially in pharmacovigilance, biomedical literature review, and Biochemistry Jobs.
Job Details
- Job Role: Associate Pharmacovigilance Specialist
- Location: Karnataka, India
- Department: Life Sciences & Healthcare
- Work Mode: Hybrid
- Job ID: JREQ135672
Key Responsibilities
- Critically analyzes large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customers’ products, as per applicable regulatory requirements and standard operating procedures.
- Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article.
- Demonstrates understanding of the client’s drug labels and uses that knowledge effectively when performing the safety assessments.
- Completes drug safety review of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with the client’s standards of timeliness and quality.
- Uses a drug safety system to track all actions and assessments in an audit-ready reference history.
- Selects articles specific to the client’s interest for inclusion in the client’s product literature database per guidelines.
- Writes accurate, detailed, and complete abstracts of selected articles using good judgment regarding the level of detail required and excellent organization, grammar, and syntax.
- Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from the client’s database.
- Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.
- Maintains an awareness of new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature.
- Participates in other duties such as searches and terminology maintenance according to business needs and per the training provided.
Qualifications
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
- A degree in Dentistry/Physiotherapy/Nursing involving patient exposure in a hospital-based environment would be an advantage.
- Certification from a professional medical writer’s association would be beneficial.
Experience Required
- At least 1–2 years of experience reviewing biomedical literature for adverse event reporting.
- OR equivalent combination of education and experience, such as an information science degree with at least 1 year of relevant working knowledge supporting drug and patient safety.
- Related experience in drug safety/pharmacovigilance is desirable.
- At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries.
- Experience with commercial and client-specific biomedical literature databases.
- A scientific/medical writing background is preferred.
Skills Needed
- Strong analytic ability to analyze and summarize biomedical case reports, studies, and scientific topics.
- Working knowledge of biomedical terminology, drugs, and therapeutic areas.
- Excellent English language skills, including comprehension, speaking, reading, and writing.
- Strong organization, grammar, and syntax skills.
- Flexibility and adaptability to changing client needs.
- Ability to maintain accurate drug safety assessments and indexing documentation.
Work Hours
Monday to Friday
9 Hours Shift
If you are searching for MSc Life Science Jobs, Clarivate Careers, or Biochemistry Jobs in pharmacovigilance and drug safety, this Associate Pharmacovigilance Specialist opportunity at Clarivate is an excellent career option for experienced Life Science professionals in India.
