Senior Associate - Medical Data Reviewer is responsible for ensuring the clinical integrity, quality, and interpretability of data generated across the clinical development lifecycle.
Candidates must possess a Masters degree in Life Sciences, Biotechnology, Microbiology, Biochemistry, Environmental Studies, Bioinformatics, or a related discipline from a recognized university. BRIC IBSD
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
Postgraduate Degree in Life Sciences, including integrated postgraduate degrees. Excellent Computer skills in MS Office, Excel, MS Word, PPT, Email video conferencing, and cloud storage.
Post Graduate Degree including the integrated PG degrees in relevant subjects (Public Health, Health Economics, Health technology assessment, Epidemiology, Biostatistics, Pharmaceutical sciences, biotechnology, biomedical engineering, Data Science or other related disciplines) with three years post qualification experience or PhD.
Applications are invited from eligible candidates for the position of Project Technical Support - III in an ICMR-funded Research Project entitled Development of In Vitro Diagnostic (IVD) Kits against drug-resistant Salmonella Infections’