March 2026

Senior, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.

Change Control Management, Deviation Management, Quality Risk Assessment. EU, MHRA, USFDA & ANVISA audits / regulatory exposure is MUST required

Sterile dosage form product development, execution and CMC submission experience for regulated markets is basic requirement.

Analytical Method Validation, HPLC - Dissolution, GC. and Analytical data review, QMS. RM & PM testing.

Participates in internship or co-op program for temporary duration. Assists andContributes to assigned team for duration of temporary internship/co-op. Receives guidance, training, and mentoring from colleagues in planning and carrying out activities and assignments.

B.A / B.Sc. / B. Com / B.Tech./B.Pharm from a recognized University with MBA or Post Graduate Diploma in Supply Chain management 

Master’s Degree from a recognized University or institute in pharmaceutical sciences, Life Sciences, Biochemistry, Microbiology any of the disciplines specified. Anusandhan National Research Foundation Scientist-H

Candidates must hold a Ph.D./Postgraduate degree in the relevant discipline. Strong academic background, research contributions, and teaching experience preferred.