(SCINPV01) Safety Data Analyst (Mumbai)
Responsibilities
- To respond to medical information queries as per SOP such as request for product leaflet, information provided in product monographs and package inserts
- To receive information and record Adverse Drug Reaction reports over telephonic call on the Telephone ADR Form.
- Perform follow-up on cases by phone and record any specific follow-up information requested by the Safety Data Analysts
- Respond to any product quality complaint as per SOP
- Assume responsibility for quality of medical data recorded and collected
Skills
- Bachelor's in Pharmacy or related science with at least 2 years of experience, or Bachelor's in Medical Science or related area, or Master's in Pharmacy or related area
- At least 1 year experience in pharmaceutical product development (formulation development, Phase 1-4 development, Regulatory affairs etc.).
- Good oral and written communication skills
- Understanding of global regulatory requirements
- Ability to work independently with minimal supervision, yet should be a good team player
- Knowledge of IT tools used in scientific data management, such as Oracle AERS, Relsys, ArisG, SAS, or others.
APPLY: Link
No comments:
Post a Comment