Site Contracts and Budget Manager

🔥 22 minutes ago

🌐 Slovakia, Poland, +3 more countries – Remote

🇸🇰 Slovakia – Remote 🇵🇱 Poland – Remote 🇷🇸 Serbia – Remote 🇷🇴 Romania – Remote 🇭🇺 Hungary – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Develop global clinical trial budget templates from complex clinical trial protocols and study documentation • Translate protocol requirements into accurate, comprehensive, and negotiation-ready global/site budget templates across multiple countries • Review protocols, amendments, SoAs, manuals, and study documentation for site-level cost implications • 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, archiving, maintenance, close-out, screen failure, unscheduled visit, participant reimbursement/travel, overhead, pass-through, and invoiceable costs • Ensure budget structures support payment terms and CTA exhibits • Incorporate country-specific cost information and benchmarks into budget templates • Establish negotiation targets, parameters, and escalation pathways • Perform detailed quality control of budget templates before release to SCM negotiators • Confirm consistency between protocol/SoA requirements and completed budgets and document assumptions • Maintain version control and auditable budget-development records • Update budgets for protocol amendments and revised study documents • Serve as a budget-development subject matter expert for SCM and study teams • Support standardization of budget templates, tools, SOPs, work instructions, and training • Identify automation and efficiency opportunities • Review, draft, negotiate, and track clinical trial, site, vendor, consulting, confidentiality, and client agreements • Resolve or escalate contractual issues with internal and external stakeholders • Track and report site contract metrics and maintain contract files and databases • Update study team members on contract negotiation and execution status • Support policies and procedures for timely contract execution

🎯 Requirements

• 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 in 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 • Proficient in MS Office software programs and computer applications • Candidates must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Fully remote work arrangement • Virtual work environment • Equal opportunity employment • Reasonable accommodation for applicants with disabilities

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