Micro Labs inviting B.Pharm/M. Pharm / M.Sc for Handling of batch manufacturing and filling activity with regulatory exposure (3 Piece, BFSeye drops and Injectable) in Sterile area.
The responsibilities include, but are not limited to, providing overall planning and strategic oversight of clinical study, including the development of detailed study plans, budget management, and coordination of Clinical Trial Coordinators across multiple sites.
Entry of clinical data into Clinical Data Management Systems and administration of documents to produce efficient, quality data management products that meet customer needs.
Post Graduate degree in Science (M.Pharm, Life Sciences, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research is mandatory with minimum 2 years experience in Clinical Trials.
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