Found Description
Senior Clinical Scientist
As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities
- Contribute to the development and creation of clinical trial protocols following high scientific and clinical standards and applicable regulations.
- Contribute to the identification, formulation and implementation of amendments to the clinical protocol, in close collaboration with the clinical lead.
- Contribute to the creation of study‑level documents, including preparation of clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers.
- Contribute to the review and writing of clinical trial documents for CTR activities, and publications (if applicable).
- Support pharmacovigilance activities such as contributing to aggregate reports, patient nar...