Plans and coordinates activities to ensure regulatory lifecycle management activities and approvals are achieved by the Local Operating Company in a timely manner for all globally approved products.
Bachelor of Pharmacy Should have experience in working in Hospitals, Clinics, Pharmacies, in case B.Pharma candidate is not available, Diploma in Pharmacy candidates with at least 02 years of experience will be considered. Computer knowledge is mandatory.
M.Pharm, Pharm.D, BDS Postgraduate in registered life Sciences. Min 2 - 4 years relevant experience into Pharmacovigilance case processing and related activities in alignment with patient safety operations.
The applicant should be an Engineering Graduate, Chartered Accountant, Cost Accountant, Post Graduate, Graduate with MBA, PGDIM from a leading institute
Support DM Delivery Leads to maintain CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data transfer agreements, and other study administrative needs.
Create and review regulatory documentation for Drug, Device and Combination product renewals and other life cycle maintenance-related submissions. Track status and progress of regulatory documentation.
Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner.
Conduct in-depth research and analysis of rare disease markets, including competitive landscape, market dynamics, and emerging trends. Develop and maintain a comprehensive understanding of the rare disease market, including key players, product portfolios, and future opportunities. Collaborate with cross-functional teams to gather and synthesise relevant data and insights to support strategic decision-making.