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Precision For Medicine

Senior Contracts Manager – FSP

Precision For Medicine

Senior Contracts Manager managing site contracts and budgets in Europe for Precision for Medicine. Collaborating closely with Clinical Operations and ensuring contract management processes.

Posted 4/15/2026part-timeRemote • 🇪🇸 SpainSeniorWebsite

About the role

Key responsibilities & impact
  • Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments.
  • Works closely with Clinical Operations study teams and plays a key role to ensure deliverables are in alignment with defined study timelines.
  • Establish process and procedures for overall site contract management in the organization.
  • Review, draft and negotiate a variety of agreements including site contracts, confidentiality agreements, and other client contracts.
  • Escalate and resolve complex issues with clients and internal stakeholders.
  • Negotiate site budget.
  • Provide guidance to business teams regarding operational implications of contract terms.
  • Ensure adherence to company policies, procedures and contracting standards.
  • Update relevant study team members regarding the status of contract negotiations and execution.
  • Establish, track, report and manage site contract metrics.
  • Coordinate execution of agreements and track agreement expirations and other obligations.
  • Support the maintenance of contract files and databases, including contract archiving.
  • Assist in designing and implementing policies and procedures to affect the timely execution of contracts.
  • Recognize where processes can be improved and take corrective action.
  • Mentor and/or Ambassador for new SCMs and Precision for Medicine staff
  • Other tasks, as assigned.

Requirements

What you’ll need
  • Graduate, postgraduate, 4-year college degree
  • Equivalent experience ideally in a scientific or healthcare discipline
  • Previous CRO experience
  • 5+ years Oncology experience
  • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements and site Budget negotiations, but no less than 7 years’ experience.
  • Experienced leading interactions with US/European/APAC or other regions institutions
  • Experienced leading interactions with Study Teams and Sponsor

Benefits

Comp & perks
  • Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
contract negotiationlegal agreements draftingclinical trial agreementssite budget negotiationcontract managementcontract metrics trackingcontract archivingprocess improvementpolicy implementationstakeholder communication
Soft Skills
mentoringproblem-solvinginterpersonal communicationteam collaborationguidance provision