Associate Director, Medical Writing

The Associate Director, Medical Writing at Structuretx will lead the medical writing team, overseeing the development of clinical and regulatory documents. This role is integral to ensuring the accuracy and compliance of all medical communications within the company.

Key responsibilities include managing the creation of clinical study reports, protocols, investigator brochures, and regulatory submissions. The Associate Director will collaborate closely with cross-functional teams to ensure timely and high-quality document delivery.

Candidates must possess a minimum of 7 years of medical writing experience in the pharmaceutical or biotechnology industry, with at least 3 years in a leadership role. A strong understanding of regulatory requirements and excellent project management skills are essential.

Structuretx offers a competitive compensation package, including health benefits, retirement plans, and opportunities for professional development. The company fosters a collaborative and innovative work environment, encouraging growth and advancement within the organization.