Medical Writing Services

RESQ Medical Writers possesses experience in all clinical trial phases and in many therapeutic areas. Our medical writing experience includes protocols, clinical study reports, investigator brochures, annual IND safety reports, manuscripts, abstracts, serious adverse event, subject discontinuation narratives, and other regulatory amendments/ submissions. Our Medical Writers coordinate the internal and external approval of materials, as well as compile feedback via successive drafts, as requested by the Client.

In order to provide the Client with the highest quality deliverables, RESQ’s medical writing services include strict quality control procedures including copy editing, proofreading, and fact checking using primary references.

RESQ Medical Writers are Detail Oriented and have Broad Experience

RESQ Medical Writers have at least Bachelor’s degrees and typically Masters degrees in a scientific discipline. They have excellent grammar and proofreading skills and are thoroughly familiar with APA and AMA editorial styles.  In addition to a required 2-5 years of biopharmaceutical medical writing experience, RESQ requires they possess a robust background in life and clinical sciences.

RESQ also believes it is important that our Medical Writers have strong project management skills, enabling them to develop and execute work plans that meet project objectives and timelines. In addition to superb written skills, our Medical Writers are impeccably well organized, detail-oriented. They possess excellent verbal communication skills, thus enabling them to thrive in a dynamic and fast-paced team environment.