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Leads a team or complex scope of work to ensure high quality delivery of innovative protocols and data packages for CSRs and Regulatory Filings. Oversees all clinical studies...
Responsible for all operational aspects of clinical trial oversight including the delivery of every study on time within budget and scope in compliance with GCP’s, SOPs and...
The Associate Director, Regulatory Affairs Marketing Authorisation is primarily responsible for providing strategic and operational direction, oversight and hands-on, day-to-day...
LINK Medical is searching for a Senior Clinical Project Manager (CPM) in all our other Swedish offices, Oslo, Copenhagen and Berlin to manage a global study. As a CPM you will be...
Lead the individual case safety report (ICSR) management and processing team at Daichi Sankyo Europe (DSE) which focuses on ICSR case handling. Performing Data Management of...
Do you have a flair for organizing and directing the documentation for regulatory submissions? Are you motivated by contributing to making a difference by working in a vaccines...
Lead and manage the entire registration process in ensuring approvals of new products, manufacturing permits, import permits, and amendments to products. Lead regulatory strategy...
Representing GRA in the Global Project Core Team and chair the Global Regulatory Project Team for key development projects within the RMMH portfolio, providing regulatory strategic...
Manage all regulatory work related to Reckitt’s Health Business Unit’s products (e.g.: OTC, biocides). Ensure compliance with all local regulations and with company Regulatory,...
The Country Medical Affairs Director DACH will lead, continuously develop, and be accountable for the country Medical Affairs function and team, ensuring Medical Affairs represents...
The incumbent is a Medical Director within a pipeline program and will be responsible for supporting clinical trials and the development strategy. The successful candidate should...
The Clinical Trial Manager is responsible for the day-to-day leadership and management of monitoring services for clinical projects, including direct communication and interaction...
You strengthen roles and responsibilities for individual team members incl. performance reviews and development plans; You define and prioritize individual deliverables across the...
Serves as interface between Company, sponsors, vendors, and other departments in the area of Safety and Pharmacovigilance; Line management responsibilities for Safety and...
Provide best in class regulatory support & input throughout the whole Innovation process with product ideas ranging from food supplements (based on vitamins, minerals,...
Providing leadership for all Quality activities related to the mammalian organization; Sets the strategy of the quality function for mammalian manufacturing, developing and...
Responsible for leading the development and delivery of innovative global regulatory strategies for an assigned global product. Oversight of global regulatory activities (where...
Develop global regulatory CMC strategies to ensure acceptance, rapid review and approval of marketing applications, supplements/variations, clinical trial applications and other...
The Director/Senior Director, Medical Affairs is responsible for providing strategic and operational leadership to the Medical Affairs function for the respective country or region...
The Head Medical Affairs follows the medical aspects of the lifecycle process of a product: from clinical trials to post-marketing studies. He/she ensures medical contact persons...
The Clinical Program Leader (CPL) leads and manages the cross-functional clinical program team, and ensures delivery of clinical activities to agreed timelines, budget and quality...
Sr, Director, Statistical Programming provides leadership in building, engaging, and growing the EU Statistical Programming team working closely with Stats Programming Leadership...
The Director, Regulatory CMC will be responsible for building an international arm of the Seagen Regulatory CMC group and immediately managing and developing staff in the EU and...