Clinical Research Nurse

Bodyline Medical Wellness Clinics; Manchester; Hybrid; GBP 28,000 - 40,000; Full time

Job summary

A leading clinical research group in the UK is looking for a Clinical Research Nurse to manage clinical trials and ensure the delivery of high-quality care. The ideal candidate will be a Registered Nurse with at least two years of clinical research experience and possess a GCP certification. You will coordinate trials, recruit participants, and support patient safety. This role offers an opportunity to work in a community-focused environment aimed at enhancing health outcomes in metabolic and women's health.

Qualifications

• Must be a Registered Nurse with NMC registration.
• 2+ years of clinical research experience required.
• GCP certification is a must.
• Strong communication, attention to detail and organisational skills are essential.
• Proficiency in Microsoft Office.

Responsibilities

• Coordinate and manage clinical trials (Phase II-IV).
• Screen, recruit and consent participants in accordance with GCP.
• Conduct research visits and monitor for adverse events.
• Screen, recruit and consent participants in accordance with GCP.
• Monitor adverse events and manage investigational products.
• Maintain source documentation and trial records; liaise with teams.
• Ensure protocol, GCP and SOP compliance; support ethics submissions.
• Participate in audits, inspections and continuous improvement.

Skills

Strong communication

Attention to detail

Organisational skills

Compassionate and patient-centric approach

Organisational skills

Independent & team work

Compassionate patient-centric approach

Clinical sample processing

Education

Registered Nurse (NMC)

GCP certification

Clinical research experience (minimum 2 years)

Tools

Microsoft Office

Digital collaboration tools (e.g., Microsoft Teams)

eISF platforms

Job description

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