
Clinical Research Associate, UK
- United Kingdom
- Permanent
- Full-time
- Contribute to the selection of potential investigators.
- Provide the required monitoring visit reports within required timelines
- Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
- Perform source data verification according to SDV plan and ensure data query resolution
- Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
- Train, support and advise Investigators and site staff in study related matters.
2 years') working as a UK clinical research monitor (or CRA), and already residing within the UK (with appropriate right-to-work in the UK already granted, if applicable)Driving License.#LI-Remote#LI-DB1