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Zealand Pharma

  • 2860Søborg,Danmark
Zealand Pharma 2860Søborg,Danmark
Job Profile Responsibilities include to: Create and guide clinical development plans for selected projects, in close collaboration with project teams Work in accordance with applicable guidelines and regulatory plans/regulatory advice to ultimately support marketing authorizations Provide relevant post-approval medical and life-cycle support Create clinical trial outlines ensuring fit for purpose design excellence in accordance with strategy and the needs of early and late-stage drug development projects Support execution of the strategy and other project related tasks on-time and with the highest quality Support the clinical team in executing the clinical development plan Act as Zealand’s medical expert for selected clinical projects and trials Ensure proper medical monitoring, including when the role is delegated to appropriately qualified medical personnel, such as outside consultants or CROs in accordance with SOPs Provide medical subject matter expertise to the clinical and...