Site Contracts Manager

Precision For Medicine

. Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts .

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating Clinical Trial Agreements and Vendor Contracts, while effectively managing contract metrics and collaborating with study teams to ensure compliance with timelines and standards.

Highest-signal resume keywords

Clinical Trial Agreement NegotiationVendor Contract ManagementContract Metrics TrackingMS Office ProficiencyRelationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract DraftingContract NegotiationSite Budget NegotiationProcess ImprovementContracting Plans Development

Soft Skills

DiscretionTeam CollaborationIndependent Work

Tools & Technologies

Contract DatabasesMS Office Software

Industry Keywords

CROHealthcareStudy TeamsSponsorsClinical Operations

About the role

Key responsibilities & impact

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 procedures for timely contract execution
Identify process improvement opportunities and take corrective action
Collaborate with Clinical Operations study teams to align deliverables with study timelines
Perform other assigned tasks

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 Sponsors
Proficiency in MS Office software programs and computer applications
Ability to work independently and in a team environment
Ability to handle sensitive issues with discretion
Preferred: Bachelor’s degree in law, scientific fields, business administration or equivalent degree
Preferred: Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations
Preferred: Successful relationship management with study teams and/or CRAs/Start-up Associates/(S)BSCAs to meet study timelines

Benefits

Comp & perks

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