Site Contracts Manager

• Review, draft, negotiate and track confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements
• Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts
• Work with supervisors and internal/external stakeholders to resolve or escalate contractual issues
• Ensure adherence to company policies, procedures and contracting standards
• Update study team members on contract negotiation and execution status
• Establish, track, report and manage site contract metrics
• Support maintenance and archiving of contract files and databases
• Assist in designing and implementing policies and procedures for timely contract execution
• Identify process improvements and take corrective action
• Perform other assigned tasks

• Graduate, postgraduate, 4-year college degree
• Experience in a CRO/healthcare field
• At least 5 years’ experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations
• Experience leading interactions with Study Teams and Sponsor
• Proficiency in MS Office software programs and computer applications
• Must be legally authorized to work in the country of employment without employer sponsorship
• Strong organizational and written communication skills
• Ability to multitask, prioritize, and execute time-sensitive matters accurately
• Ability to work independently and in a team environment
• Knowledge of contract plans/guides for CTA and budget negotiations is preferred
• Bachelor's degree in law, scientific fields, or business administration is preferred

• Fully remote work arrangement
• Equal Opportunity Employer
• Reasonable accommodation during the application process