**Responsibilities/Job Duties**
As a fundamental member of our clinical research teams, you will support the setup, execution, and closure of clinical trials in the UK.
Your tasks and responsibilities will include:
1. Being the main point of contact for hospital sites/staff (Investigators/Doctors/Nurses/Trial coordinators) to support with any queries or issues on clinical trial protocols
2. Working closely with experienced Clinical Research Associates and Start-Up Specialists to support with tasks such as obtaining missing documents, information on patient status
3. Performing initial outreach and feasibility for potential new clinical trials in the UK and Ireland
4. Processing amendments for clinical trial protocols by submitting to regulatory authorities (e.g. MHRA) and ethics committees
5. Reviewing study updates provided by the Project team to ensure required tasks are completed
6. Reviewing the electronic Case Report Forms (database where patient data is collected) to identify missing or incorrect data, and following up with sites to correct data to ensure clinical trial integrity
7. Liaising with hospital sites to ensure they have enough clinical trial supplies for patient visits