Skills: Clinical research, MD, Phase 1, Phase2, Phase 3
Mission Statement:
The Medical Director role will include responsibility for developing clinical development plans which result in a successful clinical development program. You will be medical monitor for all cardiovascular trials and will support the preparation of registration submissions.
Responsibilities:
• Act as medical lead for assigned product development programs - this includes designing clinical trials and an overall clinical development strategy.
• Interpret results of Phases I-III clinical investigations in preparation for new drug applications to relevant regulatory authorities.
• Develop, draft and/or review clinical study reports and manage the presentation of key clinical findings to internal and external constituents.
• Provide clinical development support for company activities and manage physician consultants and collaborators for each clinical research program.
• Contribute in an active and ongoing manner to the scientific, clinical and commercial development of current and future product candidates (internally and externally developed).
• Establish productive, interactive relationships with key internal departments, as well as the medical and scientific community.
• Support on-going business development efforts by providing medical and scientific input for the due-diligence process.
