Site Contracts Manager

Position Summary:

• Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements.
• Work closely with Clinical Operations study team and play a key role to ensure deliverables are in alignment with defined study timelines.

Essential Functions:

• 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.
• Update relevant study team members regarding the status of contract negotiations and execution.

Qualifications:

• Graduate, postgraduate, 4-year college degree.
• Experience in a CRO/healthcare field with at least 5 years in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations.
• Experienced leading interactions with Study Teams and Sponsor.

Skills and Competencies:

• Strong organizational/written communication skills and ability to multi-task in a fast-paced environment.
• High self-motivation and ability to work independently and in a team.
• Proficient in MS Office software and computer applications.