At a Glance
- Tasks: Coordinate clinical trials and support researchers in maintaining compliance.
- Company: Great Ormond Street Hospital, a leading paediatric research institution.
- Benefits: Competitive salary, permanent contract, and opportunities for career growth.
- Other info: Diverse workplace encouraging applications from all backgrounds.
- Why this job: Make a real difference in children's health through innovative research.
- Qualifications: Degree in science or medical field, GCP certification, and clinical trial experience.
The predicted salary is between 47951 - 56863 £ per year.
Job Overview
This full-time onsite position offers career growth opportunities within Research and Development, Grade Band 6, permanent contract, 37.5 hours per week. The role requires a commitment to travel for multi-centre trials and supports researchers to maintain GCP compliance.
Responsibilities
- Trial Start‑Up: work with the Clinical Trials Manager to plan oversight activities; prepare study documentation, Trial Master and Site Files, electronic R&D files; assist with ethics and regulatory submissions; conduct site initiation visits and central monitoring to verify investigator qualifications and resources; ensure trial supplies are adequate; liaise with the clinical trial pharmacist; identify monitoring risks and write monitoring plans.
- Trial Commencement and Monitoring: support day-to-day trial conduct, ensure protocol and SOP compliance, maintain regulatory documentation, monitor investigator staff training and communication with MHRA, HRA, DH, and other stakeholders.
Essential Criteria
- Degree in science or equivalent, or first degree in medical/biomedical subject.
- GCP certification (ICH-GCP).
- Good knowledge of UK legislation for medicinal product trials and GCP.
- Experience in a clinical trial environment (pharma, NHS, university) or practical monitoring/auditing experience.
- Understanding of NHS R&D structure and sponsor functions.
- Excellent communication, presentation, report-writing and IT skills (including databases).
- Strong organisation, negotiation and prioritisation skills.
- Self-motivated with ability to work independently, adapt to change and lead teams.
- Commitment to team working, proactive perseverance, mentor senior academic staff.
Desirable Criteria
- Audit or trial monitoring certification.
- Experience with pharmacovigilance.
- Knowledge of Department of Health policy framework for health and social care research.
Benefits
Full time, permanent contract with salary £47,951 – £56,863 per annum. Living Wage Employer. Opportunity to work with a leading paediatric research institution.
Equal Opportunity
The hospital is committed to diversity and encourages applications from under-represented groups, including BAME, disabled, LGBTQ+ and women. All applications are assessed on merit.
Clinical Trials Co-ordinator at GREAT ORMOND STREET HOSPITAL in London employer: Great Ormond Street Hospital
Great Ormond Street Hospital is an exceptional employer, offering a dynamic work environment that fosters professional growth and development within the field of paediatric research. With a commitment to diversity and inclusion, employees benefit from a supportive culture that values collaboration and innovation, alongside competitive salaries and the opportunity to contribute to groundbreaking clinical trials in a world-renowned institution located in the heart of London.
Contact Details:
Great Ormond Street Hospital Recruitment Team
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