
Study Coordinator
- London
- Permanent
- Full-time
- Perform accurate and timely data entry into study systems.
- Manage and resolve data queries in collaboration with site staff and CRAs.
- Support day-to-day study operations, including scheduling patient visits and maintaining documentation.
- Ensure compliance with study protocols, GCP, and site SOPs.
- Act as a liaison between site staff, sponsor, and CRO teams.
- Assist with monitoring visits, audits, and site readiness activities.
- Previous experience as a Study Coordinator, Research Nurse, or Clinical Research Professional.
- Strong background in hospital-based clinical studies.
- Knowledge of GCP and clinical trial regulations.
- Excellent organizational and communication skills, with strong attention to detail.
- Ability to work independently while collaborating effectively with cross-functional teams.
- Experience in oncology and/or infectious disease studies.
- Familiarity with electronic data capture (EDC) systems.
- Competitive compensation and benefits.
- Opportunity to work on impactful studies in a collaborative international environment.
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