Drug Safety Associate
4 days ago
**Date**:2 Sept 2025
**Location**:Bangalore, KA, IN
- Job Description-
- Must Have- Associate - Pharmacovigilance Officer I You will be responsible for: "Confirm validity of case by identifying minimum criteria for case creation.
- Perform duplicate search to create either an initial case or a follow-up case.
- Understanding the principles and concepts associated with patient safety case-handling process including regulatory requirements for reporting individual case safety reports.
- Identify serious adverse events and special scenario cases which includes lack of efficacy, exposure, and pregnancy case, at risk cases, and product quality complaint only cases.
- Attach the relevant source documents or any safety information/queries/follow-up information that is relevant to the case.
- Facilitate follow-up based on queries from Data entry/QC/MR or based on inconsistent/missing information in the source file. Responsible for coding which includes adverse event, medical history, Lab data, Indications etc using standardized terminology from a medical coding dictionary, such as MedDRA.
- Code products (Suspect/co-suspect, Concomitant) as per Client conventions and Regulatory requirements.
- Draft narratives." Your impact: About you: (Desired profile) Must have: Understand the principles and concepts associated with case-handling process and overall Drug Research Process.
- Cognitive abilities including verbal reasoning, attention to detail, and critical and analytical thinking.
- Good knowledge on therapy area/medical terminology.
- Good comprehension skills.
- s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
- Good to have- EQUAL OPPORTUNITY
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