We are expanding, and we are excited to launch our brand-new clinic in Warrington. We are looking for a motivated and detail-oriented Clinical Trial Rater to join our growing team. This is a fantastic opportunity to play a key role in setting up a new site, working alongside senior leadership to implement processes and systems, before moving into a clinical trial rating role as part of our dedicated team.
As a Clinical Trial Rater, you will be responsible for supporting the delivery of high-quality clinical research at our Warrington site. You will contribute to both the clinical and operational aspects of trials, ensuring compliance with protocols, maintaining the highest standards of patient care, and supporting the successful launch of the new clinic.

ABOUT YOU

We are looking for someone with a strong interest in clinical research who can combine attention to detail with excellent communication and teamwork skills. You will be adaptable, eager to learn, and comfortable working in a dynamic, evolving environment.

ESSENTIAL SKILLS & EXPERIENCE:

• Degree in a relevant Life Sciences field (e.g. Psychology, Clinical Psychology).
• Strong communication skills (verbal and written).
• Ability to use electronic systems (Microsoft 365, CTMS, study databases).
• Proven ability to deliver high-quality work within deadlines.
• Strong attention to detail and accuracy.
• Ability to work well both independently and within a team.
• Flexibility to travel to our Glasgow site for training/ad-hoc purposes (with prior notice and expenses reimbursed).
• Commitment to Good Clinical Practice (GCP) compliance and ongoing development.

• Conducting participant assessments in line with study protocols and training.
• Processing and packaging biological samples (blood/urine) including dry ice preparation.
• Making appointments, reminder calls and managing subject bookings.
• Accurately documenting clinical trial procedures in accordance with study protocols.
• Checking medications to ensure they are appropriate to the patient and are unexpired.
• Isolation and appropriate disposal / return of used medications and instruments in accordance with study protocols.
• Providing assistance as required to monitors and other auditors on site.
• Contribute to SOP development, review, and compliance.
• Maintain cleanliness, equipment calibration, and housekeeping standards.
• Support with multi-role responsibilities during the early start-up phase, including reception duties when required.