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This is an exciting opportunity to join EMS Healthcare as a Clinical Research Study Coordinator and play a key role in delivering high-quality clinical trials focused on obesity and metabolic health across the Wirral. Working within EMS’ mobile research infrastructure, you will coordinate study operations, engage with participants, and help ensure smooth study delivery in line with protocols and regulatory requirements. This is a full-time, Monday to Friday, permanent position, offering the chance to gain hands-on experience in a high-profile obesity study while contributing to a broader range of EMS clinical research activities. The role is ideal for someone with prior experience coordinating clinical research studies who is confident working independently in a fast-paced, participant-focused environment. You will have the opportunity to make a meaningful impact on research that improves patient outcomes, while developing your skills within a supportive, multidisciplinary team committed to excellence in clinical research.
Job Responsibility:
Coordinate day-to-day operational aspects of assigned clinical studies, ensuring alignment with protocols, GCP, and EMS SOPs
Schedule and manage participant visits, including screening, enrolment, and follow-up activities
Maintain detailed, accurate study documentation, including source data, CRFs, logs, and regulatory binders
Collaborate with clinical staff, including nurses and investigators, to ensure study timelines and objectives are met
Support participant retention and compliance through effective communication and follow-up
Assist in the setup and maintenance of study equipment, supplies, and site readiness
Liaise with the data management team to ensure timely entry, verification, and query resolution
Participate in site meetings, staff training, monitoring visits, and audits as required
Ensure participant safety, confidentiality, and adherence to ethical and regulatory standards
Contribute to continuous improvement and operational excellence across the EMS Study portfolio
Requirements:
Experience coordinating or supporting clinical research studies in an NHS, academic, or commercial setting
Understanding of ICH-GCP and regulatory frameworks governing clinical trials
Demonstrated ability to manage participant interactions and study workflows
Strong organisational skills with the ability to manage competing priorities
Confident using electronic data capture systems or clinical databases
Full UK residency and right to work
Valid UK driving licence and willingness to travel across Greater Manchester and EMS sites as needed
Flexibility to work early mornings, evenings, or weekends depending on study needs
Nice to have:
Experience working in obesity, metabolic health, or lifestyle-related trials
Familiarity with community-based or mobile clinical research delivery models
Prior experience working with underserved or diverse populations
What we offer:
Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years
Buy & Sell Holidays
Enhanced Maternity and Paternity Leave
1 Occasion Day each year
Healthshield
Cycle to Work Scheme
Tech Scheme
Electric Car Scheme
Subsidised company events and gatherings
A gift for your birthday
Well being support from our qualified Mental Health First Aiders, as well as via our health scheme