Associate/ Pharmacovigilance Specialist
Clarivate
Work from Office
Full Time
Min. 2 yearsJob Description
Associate/ Pharmacovigilance Specialist
Job Responsibilities:
Conduct structured searches of scientific literature databases, including PubMed, Embase, and others, using predefined search strategies and keywords.
Screen search results to identify relevant safety information, including adverse events, safety signals, and emerging risks associated with assigned products.
Conduct a secondary evaluation of screened references.
For articles of interest, index and write accurate, detailed and complete abstracts using good medical judgement and syntax.
Works closely with Manager/Senior Manager to manage stakeholders expectations.
Minimum Qualifications:
Bachelor's degree or equivalent in Pharmacy, Life Sciences, Nursing, or related field
2 Years of Relevant Experience
Job Category Summary:
Pharmacovigilance literature screening involves the systematic review of scientific and medical publications to detect adverse drug reactions and ensure drug safety. Professionals in this field critically assess research articles, clinical trial data, and other relevant literature to identify potential safety signals and maintain regulatory compliance.
At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
Experience Level
Mid LevelJob role
Job requirements
About company
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