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 • SlovakiaMid-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 adherence to company policies and timelines. Proven ability to manage contract metrics and improve processes while maintaining effective communication with study teams and stakeholders.

Highest-signal resume keywords

Clinical Trial Agreement NegotiationVendor Contract ManagementContract Metrics TrackingMS Office ProficiencyOrganizational Skills

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

Written CommunicationMultitaskingAttention to DetailDiscretionTeam Collaboration

Industry Keywords

CROHealthcareClinical OperationsStudy TeamsStakeholder Management

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 procedures for timely contract execution
Identify process improvements and take corrective action
Work closely 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 of relevant experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations
Experience leading interactions with Study Teams and Sponsors
Proficient in MS Office software programs and computer applications
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 handling of relationships with study teams and/or CRAs/Start-up Associates/(S)BSCAs to meet study timelines
Strong organizational and written communication skills; ability to multitask and prioritize
Ability to execute time-sensitive matters accurately and with attention to detail
Ability to work independently and in a team environment
Ability to handle sensitive issues with discretion
Ability to work cooperatively in a virtual environment

Benefits

Comp & perks

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