You will also contribute to advisory boards to ensure there is engagement with site-specific KEEs to ensure robust study designs, recruitment strategies.
Essential Skills/Experience:
Bachelor’s degree with focus on life sciences or equivalent
Industry or academic experience in drug development
Detailed knowledge of GCP and other regulations governing clinical research.
General knowledge of 1) medical monitoring 2) Regulatory approval process in relevant countries; 3) pharmaceutical industry/R&D operations; 4) marketing and commercial fundamentals.
Ability to grow and maintain a high level of expertise in oncology therapeutic area.
Drug Development/Clinical Development Planning: Demonstrates the ability to undertake the planning, and timely organization of components of the clinical development plan and work with other functions to achieve successful study initiation and execution.
Ability to drive/contribute to protocol design, writing and implementation
Demonstrates solid understanding of methodology in the design, conduct, review and interpretation, and presentation of clinical research.
Desirable Skills/Experience:
Ph.D. degree in life sciences (preferred)
Emerging leadership skills with the ability to influence others and drive consensus building
Emerging communication & presentation skills to communicate scientific concepts/data clearly and crisply in team settings and in formal presentations to leadership committees both internally and externally
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