Clinical Site Contracting Coordinator
ICON · UK +5 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Clinical Site Contracting Coordinator to manage site-level agreements and confidentiality disclosures across multiple European regions. The role involves contract routing, quality control, stakeholder coordination, and vendor negotiations within a sponsor-dedicated clinical research environment.
What they're looking for
- Bachelor's degree or advanced degree in relevant field
- 1–2 years of clinical research or contract management experience
- Experience supporting regulatory inspections, audits, or compliance activities
- Proficiency in Microsoft Word, Excel, Outlook, Teams, and videoconferencing tools
- Strong written and verbal communication skills
- Meticulous attention to detail and organizational abilities
- Experience with process development (SOPs, work instructions) preferred
What you'll be doing
- Route and process site-level agreements for execution via paper or digital platforms
- Perform quality control to verify signatures, dates, and protocol consistency
- Distribute executed agreements to relevant internal and external stakeholders
- File agreements in electronic repositories and update Medidata systems
- Generate reports and analytics for the site contracting management team
CompensationCompetitive base salary and performance-related incentives
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.