Company Description
The (Senior) Director Clinical Development is responsible for shaping, developing and executing the clinical development strategy for the assigned product.
Specific responsibilities include: design of clinical trials (any phase as required by the clinical development program, including phase IV), clinical protocol development, medical monitoring of clinical trials, analysis of study data, contribution and review of clinical study reports, of clinical modules of registration dossiers, of briefing books for interactions with Health Authorities.
The (senior) Director Clinical Development will represent and defend the clinical strategy during in the MAA regulatory review process across multiple geographies and in meetings with Health Authorities.
The individual will closely work with other RD functions to ensure the successful progress of projects and clinical trials and will interact with the scientific and patient community to ensure their insights are adequately incorporated in the clinical trials.
This position will require representing Sobi clinical development strategy externally as well as in internal meetings with senior management if required.
Essential to success is a strong clinical development background with previous experience in late stage clinical trial design and conduct and in major regulatory submission (e.g. EU, Canada, Japan); excellent medical knowledge in lipidology and cardiovascular, ability to build and maintain strong relationships with study investigators / key opinion leaders (KOLs), and ability to collaborate crossfunctionally.
Including, but not limited to the following:
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