Site Contracts Manager

Precision For Medicine

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

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating Clinical Trial Agreements and Vendor Contracts, with a strong focus on organizational skills and effective communication. Proven ability to manage contract metrics and ensure compliance with company policies in a fast-paced healthcare environment.

Highest-signal resume keywords

Clinical Trial Agreement NegotiationVendor Contract ManagementContracting Plan DevelopmentMS Office ProficiencyStakeholder Communication

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 SkillsAttention to DetailMulti-taskingDiscretion

Industry Keywords

CROHealthcareStudy Team InteractionClinical Study AgreementsConfidentiality Agreements

About the role

Key responsibilities & impact

Review, draft, negotiate and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments
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 policies and 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
Relevant experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, with no less than 5 years’ experience
Experienced leading interactions with Study Teams and Sponsor
Excellent organizational and communication skills and attention to detail
Knowledge of setting up Contracting Plans - Guides for CTA & Budget negotiations
Successful handling of relationships with study team and/or CRAs/Start-up Associate/(S)BSCA to meet study timelines
Strong organizational and written communication skills; ability to multi-task and prioritize in a fast-paced environment
Proficiency in MS Office software programs and computer applications
Ability to work independently and cooperatively in a virtual environment
Ability to handle sensitive issues with discretion

Benefits

Comp & perks

Fully remote work arrangement
Virtual work environment