Description
RESPONSIBILITIES:- Medically manages clinical trials to which s/he is assigned as MM
- Serves as Global Lead MM (GLMM) for pan-regional and/.or global trial(s) to which s/he is assigned
- Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc
- Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc) , review of relevant therapeutic/clinical literature and attendance in conferences and meetings
- Collaborates with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)
- Provides therapeutic and protocol-specific training to the project teams
- Provides after hours medical support for projects to which s/he is assigned
- Supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management
- Reviews and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc,) as directed by senior management
- Interacts with staff in other functional areas within the company to ensure the highest level of client satisfaction through successful execution of project
- AMONG OTHER DUTIES
In order to be considered for this position, all candidates will need to have current and valid eligibility to work in the UK or Europe.
Keywords: MSL Director, MSL Associate Director,Medical Monitor, Director Medical and Scientific Affairs,Medical Director - Oncology.