Job Description
Bodyline is continuing to grow its Clinical Research Trial Services, driven by our commitment to innovation, accessibility, and better patient outcomes. We are inviting Senior Clinical Research Nurses to join our dedicated, patient-focused team, supporting pioneering studies in obesity, metabolic disorders, and women's health. This role offers the chance to connect patients with new treatment opportunities, contribute to groundbreaking clinical research, and collaborate with a trusted, values-driven organisation renowned for excellence in trial management and patient care.
Bodyline is recruiting a number of Senior Clinical Research Nurses. With a focus on improving access to cutting-edge therapies and studies in the areas of obesity, metabolic disorders, and women's health, this patient centred service connects patients with new research opportunities and provides sponsors and CROs with a trusted clinical partner for patient recruitment, trial management and participant supported treatment.
Bodyline
Bodyline Medical Wellness Clinics is a leading CQC-registered clinical services and clinical research group with nearly 20 years of experience delivering patient-centred, medically supported health programmes. With seven clinics across the Northwest and a nationwide telehealth service, Bodyline specialises in obesity, metabolic and female health — offering GLP-1 weight management, hormone replacement therapy, and diagnostic health services.
Job Summary
This role plays a pivotal part in delivering high-quality clinical research across a range of therapeutic areas, with a strong focus on obesity and metabolic health. You will ensure safe, ethical, and compassionate care for study participants while supporting the efficient and compliant delivery of Phase II–IV clinical trials.
As part of a supportive, patient-first organisation, you'll help shape the future of treatment options while working within a friendly, community-focused clinical environment.
Key Responsibilities
- Coordinate and manage a portfolio of clinical trials (Phase II–IV)
- Read and interpret research protocols, manuals, and regulatory documents.
- Conduct informed discussion to educate patients and carers/families about trial procedures and expectations
- Conduct research visits and clinical assessments
- Screen, recruit, and consent participants in accordance with Good Clinical Practice (GCP)
- Manage randomisation and full accountability of investigational products
- Administer investigational products and monitor for adverse events
- Support the collection, processing, and handling of clinical samples
- Maintain complete and accurate source documentation and trial documentation
- Liaise with internal and external multidisciplinary teams
- Ensure compliance with protocol, GCP, and SOPs
- Support site initiation, ethics submissions, and trial close-out
- Participate in monitoring visits, audits and inspections
- Attend team meetings, training sessions, and contribute to knowledge sharing
- Prompt reporting of risks and issues, and contribute to continuous process improvement
- Other tasks to support clinical trial conduct, as required
Qualifications, Experience & Essential Skills
- Registered Nurse (NMC)
- Clinical research experience (5 years +)
- GCP certification
- Experience in obesity, metabolic health, or related therapeutic area
- Strong communication, attention to detail and organizational skills
- Ability to work both independently and collaboratively within a team - no line management responsibility
- Compassionate and patient-centric approach
- Competent use of Microsoft Office
- Car driver essential (Own Car) and willing to travel various clinic locations
Desirable Skills
- Experience with digital collaboration tools (e.g., Microsoft Teams, eISF platforms)
- Experience in women's health
- Clinical sample processing
