Key Responsibilities
Study Coordinator responsibilities will include but are not limited to:
- To participate in advertising for and recruitment of volunteers suitable for clinical studies.
- To screen the volunteers against the inclusion and exclusion criteria.
- To obtain clinical histories and samples following enrolment.
- To carry out and/or assist with clinical procedures within studies including: phlebotomy, blood laboratory processing and transportation.
- To instruct participants on study procedures.
- To collect and record clinical data from patients by developing and updating databases.
- To maintain accurate documentation of study events in source notes.
- To help with participant care while they are in clinical studies and liaise with study physicians as appropriate.
- To provide research participants with a point of contact for queries, questions or support.
- To help identify, record and report any adverse events.
- To contribute to monitoring recruitment progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems.
Skills and Experience Required:
- Experience in Healthcare is desirable but not essential.
- University level qualification would be an advantage.
- Fluency in English (essential)
- Phlebotomy/Cannulation skills (essential)
- Experience working within the UK healthcare structure (desirable)
- Pharmaceutical experience (desirable)
Job Types: Full-time, Permanent
Salary: £21,600.00-£23,000.00 per year
Benefits:
- Company pension
- Employee mentoring programme
- Free parking
- On-site parking
- Private medical insurance
- Sick pay
- UK visa sponsorship
Schedule:
- Monday to Friday
- Weekend availability
Supplemental pay types:
- Bonus scheme
- Performance bonus
- Yearly bonus
Ability to commute/relocate:
- Milton Keynes, MK15 0DU: reliably commute or plan to relocate before starting work (required)
Work Location: In person
Application deadline: 30/06/2023
Reference ID: BIOLUMINUX-HSW-2023
Expected start date: 30/06/2023
