- Plan & execute sourcing of comparator procurement/ restricted listed drugs.
- Execution of sourcing projects with the agreed timelines.
- Act as single point of contact with clients/ vendors for resolving queries.
- Good knowledge of international pharmaceutical market and clinical trial management.
- Knowledge of cGMP (Good Manufacturing Practices) & GCP (Good Clinical Practices).
- Act as primary point of contact for clients, providing timely and accurate communication and information for all relevant activities related to comparator projects, both internal and external.
- Participation in cross-functional business process improvement activities
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