Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives. Prior experience with Data Management.
Doctoral degree in Molecular Biology/Biochemistry/Plant Science/Life Sciences/ Biotechnology/ Bioinformatics or equivalent from a recognized university or equivalent
Bachelors degree in life sciences, pharmacy, or a related field. An advanced degree is preferred. Extensive experience in pharmacovigilance or drug safety reporting, with a strong understanding of relevant regulations and guidelines.
Post Graduate Degree in Life Sciences/ Post Graduate degree in the professional course selected through a process described through National Eligibility Test- CSIR-UGC NET including lectureship and GATE.
1st class Post Graduate Degree, Including the integrated PG Degree in Life Sciences Or 2nd Class Post Graduate Degree, Including the integrated PG Degree with PhD in Life Sciences
BS degree in Pharmacy or Life Sciences or relevant education. Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.