Clinical Research Nurse
Location: Multiple Northwest Locations
Compensation: Competitive salary
Contract: Full-time permanent
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.
As part of our continued growth and commitment to innovation, accessibility and improved health outcomes across the UK, Bodyline has expanded through a dedicated Clinical Research Trial Services and is recruiting a number of 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.
Role 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 (minimum 2 years)
- GCP certification
- Experience in obesity, metabolic health or related therapeutic area
- Strong communication, attention to detail and organisational skills
- Ability to work both independently and collaboratively within a team
- Compassionate and patient‑centric approach
- Competent use of Microsoft Office
Desirable Skills
- Experience with digital collaboration tools (e.g., Microsoft Teams, eISF platforms)
- Experience in women’s health
- Clinical sample processing
Other Information
- Seniority level: Entry level
- Employment type: Full‑time
- Job function: Health Care Provider
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