Location- Bangalore/Remote
Knowledge and Experience
- Experience in the pharmaceutical or clinical research organization industry and medical writing.
- Knowledge of regulatory documents and ICH-GCP guidelines, understanding of clinical research, and the drug development process.
- Proof reading, quality control or copyediting experience.
- Advanced word processing skills, including MS Office; software and systems knowledge or ability to learn and adapt to various IT systems; document management systems, collaborative authoring and file conversion and databases.
- Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent.
