BDS

Masters degree in Pharmacology/ Clinical Pharmacology/ Pharmacy Practice/Clinical Research. OR Pharm.D/ MBBS/ BDS from a recognized University/Institute. 1 year experience in drug safety/ Pharmacovigilance. Indian Pharmacopoeia Commission

Monitor and route incoming safety information to the appropriate project teams. Record all ICSR documentation and track cases in accordance with sponsor/customer specifications; distribute incoming mail and faxes.

M.Sc., B.E., B.Tech., B.V.Sc., B.Pharm., or equivalent degree and at least two years of post-M.Sc., B.E., B.Tech., B.V.Sc., B.Pharm. research experience, as evidenced from published papers in standard refereed journals. Bharathidasan University, Tiruchirappalli

Responsible for one or several of the following: processing of Individual Case Safety Reports (ICSRs) from various sources, Literature search and review, signal detection and management, tracking regulatory information

Having excellent knowledge of product/account to enable meaningful interactions with clients and authors, including consultancy where necessary.

Masters Degree in Public Health / Life Sciences / Clinical Research / Social Sciences / Epidemiology. All-India Institute of Medical Sciences

Senior Associate - Medical Data Reviewer is responsible for ensuring the clinical integrity, quality, and interpretability of data generated across the clinical development lifecycle.

Medical Regulatory Writer at Sanofi. Participate with support in the planning of analysis and data presentation to be used, initially in conjunction with the mentoring medical writer. 

M.Sc./ M.Pharm (PG Diploma in Clinical Research is mandatory)/ M.Sc. in Clinical Research/ MBBS/ BDS/ BAMS/ BHMS/ BUMS (PG Diploma in Clinical Research is Mandatory) or PharmD or Equivalent Qualification