Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Director of Medical Writing based in the United States.
This senior leadership role sits at the intersection of clinical development, regulatory strategy, and scientific communication, ensuring the creation of high-quality documentation that supports global drug development programs from early clinical phases through regulatory submission. The position combines hands-on scientific writing with team leadership, overseeing internal writers, contractors, and vendors while directly contributing to key regulatory documents. It plays a critical role in ensuring consistency, compliance, and clarity across clinical and regulatory deliverables that impact patient access to innovative therapies. Operating in a fast-paced biotech environment, the role partners closely with cross-functional experts to shape clinical narratives and submission strategy. It also contributes to the development of departmental infrastructure, standards, and long-term medical writing strategy. This is a highly visible role with both strategic influence and operational accountability across multiple programs.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Director of Medical Writing based in the United States.
This senior leadership role sits at the intersection of clinical development, regulatory strategy, and scientific communication, ensuring the creation of high-quality documentation that supports global drug development programs from early clinical phases through regulatory submission. The position combines hands-on scientific writing with team leadership, overseeing internal writers, contractors, and vendors while directly contributing to key regulatory documents. It plays a critical role in ensuring consistency, compliance, and clarity across clinical and regulatory deliverables that impact patient access to innovative therapies. Operating in a fast-paced biotech environment, the role partners closely with cross-functional experts to shape clinical narratives and submission strategy. It also contributes to the development of departmental infrastructure, standards, and long-term medical writing strategy. This is a highly visible role with both strategic influence and operational accountability across multiple programs.
