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Precision For Medicine

Site Contracts and Budget Manager

Precision For Medicine

. Develop global clinical trial budget templates from complex clinical trial protocols and study documentation .

Posted 11/4/2026full-timeRemote • Poland, Slovakia, Serbia, Romania, HungaryMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in developing global clinical trial budget templates and translating complex protocols into detailed budget structures. Proficient in contract negotiation and maintaining compliance with clinical trial agreements and payment terms.

Highest-signal resume keywords
Clinical Trial Budget DevelopmentContract NegotiationProtocol InterpretationCRO ExperienceMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Budget Template DevelopmentCost AnalysisClinical Trial AgreementsNegotiation ParametersQuality ControlVersion ControlSite Budget NegotiationBenchmarking DataInvoiceable CostsStudy Documentation
Soft Skills
Stakeholder CommunicationProblem SolvingCollaborationAttention to DetailContinuous Improvement
Industry Keywords
CROPharmaceuticalBiotechnologyHealthcareOncologyClinical ResearchStudy TeamsPayment TermsSite CostsAudit Compliance

About the role

Key responsibilities & impact
  • Develop global clinical trial budget templates from complex clinical trial protocols and study documentation
  • Translate protocol requirements into detailed, accurate, scalable global/site budget templates
  • Map procedures and activities to study visits and payment milestones
  • Develop per-patient, per-visit, conditional, invoiceable, and one-time study costs
  • Identify site start-up, pharmacy, laboratory, imaging, record retention, maintenance, close-out, screen failure, unscheduled visit, participant reimbursement/travel, institutional/overhead, pass-through, and invoiceable costs
  • Ensure budget structures support payment terms and CTA exhibits
  • Incorporate country-specific cost information and benchmarks into global and country-level budget templates
  • Establish negotiation targets, parameters, and escalation pathways
  • Perform quality control of budget templates before release to SCM negotiators
  • Maintain version control and auditable budget-development records
  • Review protocol amendments and update master/site budget templates
  • Serve as a budget-development SME for SCM and study teams
  • Support continuous improvement and standardization of templates, tools, SOPs, work instructions, and training
  • Identify automation and efficiency opportunities
  • Review, draft, negotiate, and track clinical, vendor, confidentiality, and other contracts
  • Resolve or escalate contractual issues with internal and external stakeholders
  • Track and report site contract metrics and maintain contract files and databases
  • Support policies and procedures for timely contract execution

Requirements

What you’ll need
  • Graduate, postgraduate, or 4-year college degree
  • Experience in a CRO, pharmaceutical, biotechnology, or healthcare environment
  • At least 5 years of relevant clinical research experience, including substantial hands-on experience developing investigator/site budget templates
  • Demonstrated experience developing global and/or multi-country clinical trial budget templates for sponsor- or CRO-managed studies
  • Strong ability to interpret complex protocols, SoAs, amendments, and supporting study documents and translate requirements into complete site-level costs
  • Experience using country-specific cost information and/or benchmarking data to develop budget assumptions and negotiation parameters
  • Knowledge of CTA budget exhibits, clinical trial payment terms, and site budget negotiation processes
  • Relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts, and Site Budget negotiations
  • Experience leading interactions with Study Teams and Sponsors
  • Experience with oncology and/or other complex clinical trial protocols
  • Proficiency in MS Office software programs and computer applications
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship