Life Sciences

Post-graduate in Life Sciences (preferably Pharmacy) with minimum of 3 years pharmaceutical industry experience in regulatory affairs with proven track record and experience in health authority interactions and negotiations, end-to-end regulatory submissions

Responsible for achieving Financials & Strategic targets for Pharma & Biotech segment. Manages, coaches, and develops a team of Solution Scientists and account managers to achieve assigned goals.

Experience in the development and application of pharmacometric models to support drug development and regulatory submissions.

B.Pharm from a recognized university with experience in clinical trial monitoring or clinical site coordination & management. Clinical Development Services Agency, CDSA is a niche center of THSTI

M.Sc in life sciences, PG diploma in Clinical Research and Pharmacovigilance 

Participation in Trade Association calls in listening & learning, observer mode by leveraging the discussion and lessons learnt onto CMC Regulatory Intelligence databases.

Review of Product Quality Complaint Investigation Reports Drug Products.Coordinate with other stakeholders involved in the complaint handling process.

First Class Post Graduate Degree in Pharmacy / Professional Courses or any Life Sciences, including the integrated PG degrees.

Doctoral Degree in Life Sciences or Masters Degree in Engineering or Technology from a recognised university or equivalent.