Senior Contract Manager – FSP

Precision Medicine Group

. Establish processes and procedures for overall site contract management .

Posted 10/27/2026full-timeRemote • United StatesSenior💰 $110,700 - $166,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in contract management, including drafting, reviewing, and negotiating Clinical Trial Agreements and vendor contracts. Proven ability to mentor teams and manage complex stakeholder interactions while ensuring compliance with company policies.

Highest-signal resume keywords

Contract ManagementClinical Trial AgreementsNegotiation SkillsMS Office ProficiencyStakeholder Interaction

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

DiscretionIndependenceCooperationMentoring

Tools & Technologies

Contract DatabasesMS Office

Industry Keywords

HealthcareScientific DisciplineClinical TrialsVendor Agreements

About the role

Key responsibilities & impact

Establish processes and procedures for overall site contract management
Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts
Escalate and resolve complex issues with clients and internal stakeholders
Negotiate site budgets
Advise business teams on operational implications of contract terms
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
Coordinate agreement execution and track expirations and other obligations
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
Mentor and serve as an ambassador for new Senior Contract Managers and Precision for Medicine staff
Perform other assigned tasks

Requirements

What you’ll need

Graduate, postgraduate, 4-year college degree
Equivalent experience ideally in a scientific or healthcare discipline
No less than 7 years’ relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, vendor contracts and site budget negotiations
Experience leading interactions with US, European, APAC or other regional institutions
Experience leading interactions with Study Teams and Sponsors
Proficiency in MS Office software programs and computer applications
Ability to manage multiple priorities in a fast-paced environment
Ability to handle sensitive issues with discretion
Ability to work independently and cooperatively in a virtual environment
Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation