Description
We are currently working with a global CRO who are looking for CRA/SCRA to join them on an interim basis initially for 6 months with a strong possibility of being extended on-wards.The Role:
-Monitor activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols
-Responsible for multiple projects and must work both independently and in a team environment.
-May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings.
Key Skills:
Can consider CRA or SCRA level
-Must have minimum 2 years independent monitoring experience
-Phase 1 experience
-Therapy areas - Infectious Diseases - Autoimmune disease
Location: London / South
The hourly rate for this role is between £40-£50 depending on experience.
Please apply if interested!