1.Narrative Writers & Reviewers: With at least 4 – 5 years of experience in Regulatory Medical Writing, primarily in Narrative Writing.
2. Regulatory Medical Writers and Reviewers: With 2 - 5 years of experience in authoring, reviewing/project managing CSRs, IBs, protocols, summary documents across all therapeutic areas.
3. DSRM (Drug Safety & Risk Management) Writers and Reviewers: With 2 to 6 years of experience in authoring and reviewing of aggregate reports (DSURs, PSURs/ PBRERs, PADER etc). Experience in RMP updates and QCs would be an added advantage.
4. Clinical Trial Disclosure Writers and Reviewers: With around 2 - 4 years of experience in authoring /quality check of Clinical Trials Registration and Results (CTRR – protocol registry forms and results summaries) documents, lay summaries and review of redacted CSRs & summary documents.
Interested candidates can share their updated CV's on [email protected]