Trilogy Writing and Consulting

Lead the preparation of clinical regulatory documents such as protocols, study reports, and summaries in collaboration with client teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.

Perform quality control on clinical and nonclinical regulatory documents to ensure data accuracy and adherence to style guides. Lead complex QC projects, coordinate other specialists, and manage client interactions.

Lead the preparation of various clinical regulatory documents and scientific publications in collaboration with client authoring teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.

The Medical Writing Manager will provide line management and resource oversight for a team of medical writers while maintaining a reduced individual writing workload. They will also participate in strategic management activities, business development, and represent the company in client interactions.