Site Contracts Manager

Precision Medicine Group

. Review, draft, negotiate and track confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements .

Posted 9/15/2026full-timeRemote • SerbiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating various types of contracts, including Clinical Trial Agreements and Vendor Contracts, while ensuring compliance with company policies and procedures. Proven ability to collaborate with cross-functional teams and manage contract metrics effectively.

Highest-signal resume keywords

Contract NegotiationClinical Trial AgreementsVendor ContractsMS Office ProficiencyOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract DraftingContract ReviewContract ManagementSite Budget NegotiationContracting Plans

Soft Skills

Written CommunicationMultitaskingDiscretionTeam CollaborationProblem Solving

Tools & Technologies

Contract DatabasesMS Office Software

Industry Keywords

CROHealthcareClinical OperationsStakeholder Engagement

About the role

Key responsibilities & impact

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
Maintain contract files and databases, including contract archiving
Assist in designing and implementing policies and procedures for timely contract execution
Identify process improvements and take corrective action
Collaborate with Clinical Operations study teams to align deliverables with study timelines

Requirements

What you’ll need

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
Bachelor’s degree in law, scientific fields, business administration or equivalent degree preferred
Knowledge of setting up Contracting Plans - Guides for CTA & Budget negotiations preferred
Proficiency in MS Office software programs and computer applications
Ability to work independently and in a team environment
Strong organizational and written communication skills
Ability to multitask, prioritize, and handle time-sensitive matters accurately
Ability to handle sensitive issues with discretion
Ability to work cooperatively with others in a virtual environment

Benefits

Comp & perks

Fully remote work arrangement
Regular full-time employment
Equal Opportunity Employer
Reasonable accommodation available during the application process