Define TPP and draft CDP for the assigned projects, update the same and keep updated based on inputs from various line functions Medical monitoring of the trials, point contact for all safety and medical questions for assigned trial Will author and sign off on : Protocols, IB, IND/CTA clinical sections, briefing books, CSR, clinical dossier and publications Maintain effective relationships with key investigators to ensure high scientific quality and relevance of trial design and endpoints.
Will have direct oversight on operations team. Accountable for the trial metrics- FPFV, LPLV, DBL and CSR timelines, the medical expert will be the driver of the team performance to achieve milestones for the project.Lead investigator meetings and advisory boards
Education: MBBS, MD/MS
Deadline: Contact employer