Hybrid Director, Medical Writing

Director, Medical Writing Resourcing Group Lead page is loaded## Director, Medical Writing Resourcing Group Leadlocations: Americas, US-PA, King of Prussia, CSL Behring: EMEA, CH, Kanton Zurich, Opfikon, CSL Vifor: EMEA, GB, Berkshire, Maidenhead, CSL Behring: Americas, US-MA, Waltham, CSL Behringtime type: Full timeposted on: Offerta pubblicata...

Position Summary:We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

Position Summary:We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

Position Summary: We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

Position Summary: We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

Position Summary: We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

Description Summary:You will be responsible for the provision of medical writing services to support clinical development by way of managing the Medical Writing budget project and functional budget, as well as ensuring the medical writing team is resourced appropriately to meet the demands of the portfolio.You are the key leadership role in the Clinical...

Position Summary: We are seeking an experienced and highly motivated (Associate) Director, Medical Writing to join our Regulatory/Clinical Development team. This leadership role is responsible for the strategic planning, preparation, and delivery of high-quality clinical and regulatory documents in support of global drug development programs. The ideal...

A biopharmaceutical company in Waltham, MA seeks an Associate Director/Director of Quality Control to ensure compliance and oversee analytical testing in a GMP environment. Candidates should have over 8 years of experience in QC or analytical sciences, particularly in monoclonal antibody testing. This role offers a competitive salary between $175,000 and...

A leading manufacturing marketplace is seeking a Director of Partner Management to build and scale a high-performing Partner Network. The ideal candidate will have over 8 years of experience in manufacturing operations and a strong understanding of category-specific processes. Responsibilities include managing Partner lifecycle, ensuring compliance, and...