● Organising study set-up

● Supporting implementation of local processes and procedures

● Downloading and completing database searches

● Screening and eligibility checks

● Mail outs / Text outs

● Consent and randomisation

● F2F clinic visits, baseline observations and phlebotomy

● Transport, storage, spinning and posting of category B specimens according to

protocol and lab manual and local facilities for storing human tissue

● Advice and support on study feasibility, set-up process and study schedule

within the GP practice care pathway

● Screening and recruitment logs of study participants ensuring adherence to

GDPR

● Electronic Site Filing management and physical Site File management

● Data management including completion of paper and electronic case report

forms (CRFs)

● Liaising with Sponsor/study team on any queries.

● Identifying AEs, SAE, SUSARS, supporting PIs to complete electronic and paper

forms and guiding principal investigators through the reporting process to the

sponsor and any follow-up forms.

● SystmOne documentation

● Promotion and outreach of specific studies that may be suitable for the GP

practice

● Signposting to workforce development site (WFD) to access e-learning and

websites

● Supporting specific events to promote research within primary care, new and

existing