Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with investigative sites
Job Summary
Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with investigative sites.
Maintains consistent communication with study sites and internal stakeholders in alignment with site contracts department and client requirements.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with investigative sites.
Skills & Requirements
Must-have
Clinical trial agreements negotiation
Complex amendments management
Ancillary agreements with sites
Site contracts department communication
ICON and client systems tracking
Risk identification and mitigation
Nice-to-have
Fostering inclusive environment
Driving innovation and excellence
Shaping future of clinical development
Mentoring team members
Key Requirements
Minimum 5 years contract experience
Pharmaceutical or clinical research industry experience
Strong understanding of contract law
Excellent analytical and problem-solving skills
Strong attention to detail and organizational skills