CLARIVATE is a major player in providing the right information and various services to help businesses, researchers, and professionals make the right decisions. The company offers solutions and data for research, IPR, Pharmaceuticals, Biotech, and educational and research Institutions. For more details, please visit the official website of Clarivate
Vacancy Details
- DESIGNATION – Associate Pharmacovigilance Specialist
- DEPARTMENT – Pharmacovigilance
- DIVISION – Life Sciences & Healthcare
- EXPERIENCE – Freshers & Experienced
Associate Pharmacovigilance Specialist Job Responsibilities
- Observe and study biomedical literature for Adverse Event (AE) reporting.
- Provide accurate, comprehensive, and well-organized articles using sharp judgment skills to assess the required details and focus on excellent grammar and logical structure.
- Generate short summaries highlighting the criteria of ICSR and other safety-related information from each article.
- Utilize the knowledge of pharmacovigilance regulations, therapeutic areas, and scientific terminology.
- Determine the safety parameters of drugs for each batch of biomedical literature in a timely fashion and comply with the client’s requirements for quality and efficacy.
- Determine the individual case safety reports and other related safety details that may influence the safety profile of the customer’s product.
- Briefly extract important elements of articles and prepare detailed indexes of abstract content to verify effective and complete retrieval of literature from the client database.
- Track all records of actions and evaluations using the drug safety system to prepare an audit-ready history for future reference.
- Study and review articles from biomedical literature and internal drug safety alerts.
- Identify and pick articles related to the client’s interest for entry into the client’s product literature database and ensure compliance with regulatory standards.
Educational Qualification
- Master’s degree in Life Sciences, Pharmacy, Biomedical Sciences, Health, Biotechnology, Biochemistry, and Biotechnology.
- Clinical degree in Dentistry / Physiotherapy / Nursing
- A certificate from a professional medical writer’s institution is desirable.
- A minimum of 01 Year of Experience is required in reviewing biomedical literature for adverse event reporting.
Skills Required
- Proficiency in biomedical terminology, drugs, and therapeutic areas.
- Expertise in literature databases and scientific writing.
- Good analytical skills to determine the important points of biomedical studies and case reports.
- Experience with commercial and client-tailored biomedical literature databases.
Clarivate Associate Pharmacovigilance Specialist Salary
CLARIVATE RESEARCH AND DISCOVERY CENTRE has not disclosed the salary figures, but as per company standards and job category. The salary ranges from INR 4,00,000 to INR 6,00,000 per annum based on academic qualifications, Job profile, and experience of personnel.
Role Characteristics
Clarivate is hiring young and talented candidates with some working experience in the Pharmacovigilance department of any reputed organization. The candidates selected by Clarivate will be allowed to work in a hybrid mode with a regular full-time job opportunity. Please read the mentioned details for further information.
- Job Location – Bangalore, Karnataka, India
- Position Type – Full-Time / Regular
- Work Mode – Hybrid
- Company – Clarivate Research and Discovery Centre
- Industry Type – Clinical Research Company
How to apply for the Clarivate Associate Pharmacovigilance Analyst Job?
Candidates who qualify for the eligibility criteria of the Job role and are interested in working in the healthcare sector can apply for the post by filling out the application online. Make sure you cross-check all the details carefully before the final submission. Shortlisted candidates will be updated via mail or phone by the concerned HR department.
