Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Medical Writing based in the United States.
This is a senior scientific writing leadership role within a fast-growing clinical-stage environment focused on advancing innovative therapies for patients with severe autoimmune diseases. The position plays a critical part in shaping and delivering high-quality clinical, nonclinical, and regulatory documentation across all phases of drug development. You will lead the preparation of complex regulatory submissions, ensuring clarity, scientific accuracy, and compliance with global standards. The role combines hands-on authorship with strategic oversight of medical writing processes and standards. You will also guide and mentor a team of writers while collaborating closely with cross-functional stakeholders. This is an opportunity to influence both late-stage regulatory strategy and the evolution of internal medical writing capabilities in a highly dynamic setting.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Medical Writing based in the United States.
This is a senior scientific writing leadership role within a fast-growing clinical-stage environment focused on advancing innovative therapies for patients with severe autoimmune diseases. The position plays a critical part in shaping and delivering high-quality clinical, nonclinical, and regulatory documentation across all phases of drug development. You will lead the preparation of complex regulatory submissions, ensuring clarity, scientific accuracy, and compliance with global standards. The role combines hands-on authorship with strategic oversight of medical writing processes and standards. You will also guide and mentor a team of writers while collaborating closely with cross-functional stakeholders. This is an opportunity to influence both late-stage regulatory strategy and the evolution of internal medical writing capabilities in a highly dynamic setting.
