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TransPerfect is seeking freelance Medical Writers based in India to support preparation of clinical trial protocols, clinical study reports, informed consent forms, and investigators brochures. The role emphasizes accuracy, adherence to deadlines, and strong English writing skills.
Candidates should hold a science degree and have at least five years of experience as a Clinical Medical Writer, with proven ability to deliver high-quality documentation under tight timelines.
In order to meet the needs of our clients, we are currently looking to expand our database of Freelance Medical Writers working with clinical trial protocols; clinical study reports; informed consent forms; investigators brochures etc
Based in India
Excellent written and verbal communication skills in English
Specialized in the following subject matters: clinical trial protocols; clinical study reports; informed consent forms; investigators brochures
Acute attention to detail, spelling and grammar
Ability to maintain professionalism in all situations, especially under tight deadlines
A Science Degree
5 years experience as Clinical Medical Writer