Clinical Trials & Patient Engagement
$38,000–$52,000 year
On-siteCanary Wharf, England, United Kingdom
Job Summary
Coordinate and manage day-to-day clinical study operations, overseeing participant recruitment, screening, and consent in accordance with IRB-approved protocols. Maintain accurate source documentation and electronic data capture systems while monitoring patient safety and scheduling study visits. Liaise with principal investigators, sponsors, and ethics committees to prepare regulatory documentation, site initiation, and close-out reports. Ensure quality assurance and compliance with ICH-GCP, MHRA, and institutional regulations while tracking study progress and submitting timely updates to stakeholders.
Required Qualifications
- In-depth knowledge of GCP, clinical research regulations, and ethical standards
- Experience with clinical data collection, source documentation, and informed consent processes
- Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar)
- Strong organizational and time management skills
- Excellent communication and interpersonal abilities
- Detail-oriented and able to handle multiple trials simultaneously
Desired Qualifications
- Bachelor's degree in Life Sciences, Nursing, or Health Sciences
- ACRP or SOCRA certification
- Previous experience in oncology, cardiology, or rare disease clinical trials
- Familiarity with clinical trial software platforms and regulatory submissions
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