Freelance Clinical Medical Writer
TransPerfect
•Remote
About The Position
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.
Requirements
- Based in India
- Excellent written and verbal communication skills in English
- Specialized in 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
Responsibilities
- Writing clinical trial protocols
- Writing clinical study reports
- Writing informed consent forms
- Writing investigators brochures
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What This Job Offers
Career Level
Senior
