Site Contracts Manager

Precision For Medicine

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

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating legal agreements, particularly Clinical Trial Agreements and Vendor Contracts, while ensuring compliance with company policies and effective communication with stakeholders. Proficient in managing contract metrics and implementing process improvements to enhance contract execution efficiency.

Highest-signal resume keywords

Clinical Trial Agreement NegotiationVendor Contract ManagementContracting Plan DevelopmentStakeholder CommunicationMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract DraftingContract NegotiationSite Budget NegotiationContract Metrics ManagementProcess Improvement

Soft Skills

Organizational SkillsWritten CommunicationMultitaskingPrioritizationDiscretion

Industry Keywords

CROHealthcareStudy TeamsCRAsStart-up Associates

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
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 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 of relevant experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations
Experience leading interactions with Study Teams and Sponsor
Preferred: Bachelor's degree in law, scientific fields, business administration or equivalent degree
Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations
Experience handling relationships with study teams and/or CRAs/Start-up Associates/(S)BSCAs to meet study timelines
Proficiency in MS Office software programs and computer applications
Strong organizational and written communication skills
Ability to multitask, prioritize, work independently and in a team environment
Ability to handle sensitive issues with discretion

Benefits

Comp & perks

Fully remote work arrangement
Work in a virtual environment