
Manager, Clinical Site Contracts and Budgets
Posted Jul 31

Posted Jul 31
This is a fully remote position, open to applicants in Spain.
• Act as the primary lead for site contracts and budgets across designated studies, ensuring the timely, high-quality, and compliant execution of the site budget and contract negotiation process.
• Engage with key stakeholders on the study team from the early planning phase and throughout the contract lifecycle to prioritize, plan, and execute in alignment with operational objectives.
• Proactively drive prioritization and advancement of site contracts within the clinical trial working group.
• Develop or oversee the budget setup, incorporating study-specific parameters for assigned studies utilizing industry tools and data sources.
• Efficiently manage site contracting-related issues in accordance with established escalation pathways.
• Effectively communicate internally and with external partners to ensure alignment and excellence in the coordination of study start-up activities (e.g., SIV scheduling).
• Ensure that all relevant systems and trackers are accurate and up-to-date concerning the status of site budgets and contracts.
• Implement standards in the site budgeting and contracting process across studies/programs.
• Oversee all changes to study scope, ensuring timely execution of amendments.
• Lead initiatives for the improvement of the site budget and contract processes, as necessary.
• Manage study-level KPIs and metrics related to site budget and contract negotiation.
• Provide training and mentorship to peers and stakeholders as required.
• Collaborate with Legal, Compliance, and other partnering functions for continuous enhancement of site budgeting and contracting processes.
• A minimum of 5 years of experience leading clinical budgets and contract negotiations.
• Proficiency in both Spanish and English is essential.
• Strong skills in relationship building, negotiation, and conflict resolution.
• Proven excellence in verbal, written, and interpersonal communication abilities.
• Demonstrated understanding of clinical operations and study start-up processes.
• Experience in driving global site budget and contract strategies.
• Familiarity with common budget development and data tools (e.g., Grant Plan).
• Demonstrated knowledge of regulatory and legal matters related to the conduct of clinical trials.
• A bachelor’s degree is mandatory.
• A JD or MBA is preferred.
• Competitive salary.
• Attractive benefits package.
• Comprehensive medical care plan: Health, Dental & Vision.
• Life Assurance coverage.
• Excellent work environment.
• Culture fostering teamwork and collaboration.
• A motivated team that faces challenges together.
• Access to innovative technology.
• Outstanding training opportunities.
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