Clinical Research Contracts Specialist at ICON
ICON Strategic Solutions • quebec, Canada
Role Description
Elevate your career as a Clinical Research Contracts Specialist at ICON, where you'll manage and optimize clinical trial agreements. Engage with stakeholders and ensure compliance across contracts.
This role requires a Bachelor's degree and a minimum of 3 years of experience in contract management, particularly in the pharmaceutical or clinical research industry. Your expertise in contract law and excellent analytical skills will enable you to facilitate timely site setups while maintaining internal and external communication.
Key Responsibilities:
• Draft, review, and negotiate clinical trial agreements
• Maintain communication with study sites and stakeholders
• Track contractual progress in ICON and client systems
• Proactively identify risks and propose mitigation strategies
• Participate in departmental initiatives and mentor team members
Requirements:
• Bachelor's degree in Business or Legal Studies
• 3+ years of contract administration experience
This role requires a Bachelor's degree and a minimum of 3 years of experience in contract management, particularly in the pharmaceutical or clinical research industry. Your expertise in contract law and excellent analytical skills will enable you to facilitate timely site setups while maintaining internal and external communication.
Key Responsibilities:
• Draft, review, and negotiate clinical trial agreements
• Maintain communication with study sites and stakeholders
• Track contractual progress in ICON and client systems
• Proactively identify risks and propose mitigation strategies
• Participate in departmental initiatives and mentor team members
Requirements:
• Bachelor's degree in Business or Legal Studies
• 3+ years of contract administration experience