Review, draft and negotiate a variety of agreements including master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts
Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues
Ensure adherence to company policies, procedures and contracting standards
Update relevant study team members regarding the status of contract negotiations and execution
Establish, track, report and manage site contract metrics
Support the maintenance of contract files and databases, including contract archiving
Assist in designing and implementing policies and procedures to affect the timely execution of contracts
Recognize where processes can be improved and take corrective action
Requirements
Graduate, postgraduate, 4-year college degree
Experience in a CRO/healthcare field
Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience
Experienced leading interactions with Study Teams and Sponsor
Benefits
Precision Medicine Group is an Equal Opportunity Employer
Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law
Reasonable accommodation available for individuals with disabilities