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You will take charge of leading regulatory CMC strategy and execution for one or more transformative medicine programs. This pivotal role involves developing and implementing...
Develop and implement regulatory strategies for successful product approvals; Provide strategic guidance to cross-functional teams on regulatory requirements and risks Ensure...
The Medical Affairs Manager provides support to the Clinical Evaluation Group for ongoingly assess the safety and performance clinical data of the Bausch+Lomb Surgical Medical...
You will be responsible for all regulatory activities related to product development and marketing authorizations in the region and is the primary contact point within UCB for any...
Provision of regulatory input and support to Post-Approval Regulatory procedures in EU and ROW (document quality and accuracy, coordination of input from other line functions,...
In this role, you will be responsible for leading an operational team that provides a range of services related to laboratory analysis within clinical trials for our clients. This...
Ensure that all products in scope are designed, manufactured and distributed in such a way that they are safe and effective for their intended use and meet applicable regulatory...
Provide strategic medical safety leadership and practical contributions for assigned product(s) in a cross-functional setting; Perform safety signal management and benefit risk...
Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a...
The Director, Immunology European Medical Engagement Lead (MEL) conducts critical activities that support advancing science, educating on evolving clinical practices, transforming...
Provide strategic and technical pharmacovigilance advice to Global Patient Safety (GPS), and other regulatory and medical functions within the Medicines Development Unit; Play an...
Manage, prepare, finalise CMC sections of EU IMPD/MAA and rest of world equivalent documents. Oversee teams preparing content, arrange reviews by regulatory, SME peers, senior...
Lead design of preclinical and/or clinical studies needed to support health benefit claims. Author, update and maintain relevant scientific documentation. Work closely with Product...
As a Director, you will be responsible for the successful execution of multiple projects and ensuring client satisfaction. You will provide mentorship, leadership and direction to...
Management of cases with pharmacovigilance and materiovigilance departments. Regular training of Sales resources (place of the radiopharmaceutical in the strategy tree of...
Lead the initial development, approval, and ongoing compliance of product labeling content throughout the product life cycle; track status and maintain documents in controlled...
Responsible for providing strategic regulatory guidance on the global pediatric development in alignment with and within the overall development of a product; Lead multiple...