Skip to main content

Associate Director of Medical Writing

Posted 4 days ago

virtual vocationsDenver (CO)

SENIORITY

Lead

Apply (opens in a new tab)

About the role

Collaborating with cross-functional teams, the remote Associate Director of Medical Writing will prepare and finalize regulatory documents, manage writing timelines, and ensure compliance with regulatory requirements in a full-time capacity.
Key responsibilities: Prepare, edit, and finalize clinical and regulatory documents, including protocols and clinical study reports Interact with document authors and reviewers to gather necessary input and facilitate the document review process Participate in refining medical writing processes and ensure efficient preparation of high-quality deliverables
Required qualifications: BA/BS degree in a scientific field; advanced scientific degree (PhD, PharmD, or MS) preferred 8+ years of regulatory medical writing experience in the pharmaceutical industry Knowledge of oncology disease areas preferred Proficiency in MS Office applications, Adobe Acrobat, and electronic document management systems Ability to manage multiple projects simultaneously with minimal direction

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.

More like this