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Operations Assistant Bank
Hands-On Roles: Clinical Research Technician – 0-Hours (Bank) Position
Fortrea’s Clinical Research Unit – Leeds
Your skills in hospitality, retail, customer service, or fast-paced people-focused roles could help deliver groundbreaking new medicines—like life-saving drugs that touch many students’ lives worldwide.
Our Drapers Yard Clinical Research Unit, just 7 minutes’ walk from Leeds train station, offers bank (0-hours) flexibility with shifts matching study schedules and clinic demand. No degree required—just detail orientation, adaptability, and a curious mind. We provide full training in technical skills.
About the Role
A role where practical expertise strikes first—flexible hours (up to 37 hrs/week in busier periods, but variable) to support trials across Monday to Sunday, including weekends, twilight, and night shifts as required.
No formal scientific background needed—your experience in high-volume customer-facing environments and follow-through is what matters. Each task in this role will contribute directly to ensuring clinical trials run safely, accurately, and on time.
You’ll collaborate with nurses, doctors, and technicians as part of Phase I clinical trial teams, stepping in wherever your skills are needed.
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Who You Are
- Adept at plain English and basic maths: our core requires applying clear logic.
- Proficient in Microsoft Office: your basic Outlook, Word, and Excel skills are valuable.
- Confident with fast-paced environments: experience in hospitality, retail, or similar roles provides a jumping-off point.
- Curious & eager to learn: we’ll upskill you in essential procedures—train confidently, contribute confidently.
Key Responsibilities (Your Real-Time Impact)
Depending on live studies in progress, your varied hands-on tasks include:
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Accurate Effortless Monitoring:
- Measure blood pressure, pulse, respiratory rate, temperature, body weight.
- Handle venipuncture for blood samples.
- Prepare and document ECGs and Holter monitors.
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Protocol Followership:
- Collect, process, and distribute biological samples as required in study protocols.
- Observe and report menu compliance—ensuring study volunteers adhere to dietary timelines.
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Logistics & Support:
- Ready and sanitise patient rooms and medical equipment.
- Maintain a safe, compliant working and testing environment.
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Quality Assurance:
- Diligently record all observations, study data, and documentation.
- Help verify source documents and case reports against accuracy standards.
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All endeavours feed toward a collective mission: transforming medicines from lab to real-world impact.
Why You Apply Here Today
Forceful Career Entry Point
Gain hands-on perspective on clinical trial execution, cross-train across multiple departments, and see how studies flow from conception to regulatory submission.
Beyond the CV and Backwards:
You’ll know you helped Lay the Foundation for A Drug that Could Change Lives
Flexible, Solid-Loaded Background
- 0-hours assignment to help you balance clinical research work with other life goals.
- Continuous growth: training covers medication administration basics, student preparation, data tracking and study compliance.
- Shifts adapt to real-world research—casual availability from Monday through Sunday, requiring weekend readiness as needed.
Learn More
See diversity and EEO information, or accommodation requests here.
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