The Role
1. Promote Good Clinical Practice (GCP) in the conduct of clinical studies by adhering to protocol requirements.
2. Oversee the medical and psychiatric evaluation and management of subjects at screening and throughout their participation in clinical trials for psychedelic-assisted psychotherapies for mental health conditions, including dosing sessions and referrals to GP or specialist services if required.
3. Ensure all trial-related procedures are conducted in accordance with trial protocols, reporting and recording any protocol deviations as appropriate.
4. Ensure serious adverse events / adverse events are reported to the PI appropriately.
5. Oversee clinic personnel performing study specific tasks and procedures.
You
6. MRCPsych
7. Current ILS or ALS (can be obtained following appointment to the role)
8. At least 6 months experience as a study physician within clinical research environment
9. GCP certification (can be obtained following appointment to the role)
10. GMC full registration with licence to practise
11. Fluency in English
12. Experience working within UK health systems