Site Contracts Manager

Precision Medicine Group

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

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 collaborating with study teams and managing contract metrics. Strong organizational and communication skills are essential for ensuring adherence to contracting standards and timely execution.

Highest-signal resume keywords

Clinical Trial Agreement NegotiationVendor Contract ManagementMS Office ProficiencyContract Metrics ManagementOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract DraftingContract NegotiationSite Budget NegotiationContracting Plans DevelopmentClinical Study Agreements

Soft Skills

Written CommunicationMultitaskingDiscretionTeam CollaborationProblem Solving

Tools & Technologies

Contract DatabasesMS Office Software

Industry Keywords

CROHealthcareStudy TeamsSponsor InteractionsContracting Standards

About the role

Key responsibilities & impact

Review, draft, negotiate and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements
Collaborate with Clinical Operations study teams to align deliverables with study timelines
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 procedures for timely contract execution
Identify process improvements and take corrective action
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 Sponsor
Proficient in MS Office software programs and computer applications
Strong organizational and written communication skills
Ability to multitask and prioritize in a fast-paced environment
Ability to work independently and in a team environment
Ability to handle sensitive issues with discretion
Preferred: Bachelor's in law, scientific fields, business administration or equivalent degree
Preferred: Knowledge of setting up Contracting Plans and Guides for CTA & Budget negotiations
Preferred: Successful relationship handling with study teams and/or CRAs/Start-up Associate/(S)BSCA

Benefits

Comp & perks

Fully remote work arrangement
Equal opportunity employment
Reasonable accommodation for applicants with disabilities