Specialty
The role
TransPerfect is expanding its database of freelance clinical medical writers who work on trial protocols, study reports, informed consent forms and investigator brochures. Candidates must be based in India.
What you will do
- Write clinical trial protocols
- Write clinical study reports
- Prepare informed consent forms
- Prepare investigator brochures
What they ask for
- Based in India
- A science degree
- 5 years of experience as a clinical medical writer
- Excellent written and verbal English
- Specialised in protocols, study reports, consent forms and investigator brochures
- Strong attention to detail, spelling and grammar, including under tight deadlines
- Must complete a writing test as part of applying
What they offer
- Freelance contract
This is our own short reading of the posting. The full description, and anything that has changed since, is on TransPerfect's careers page behind the apply button.
