Sr. Site Contract and Payment Associate in Abbeyville, Colorado at Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. Site Contract and Payment Associate based in the United States.

This role offers the opportunity to support the advancement of innovative ophthalmic clinical research by managing critical site contracting and payment activities.
You will play a key part in ensuring clinical trials launch efficiently through accurate agreements, budgets, and payment processes.
The position combines contract management, financial analysis, operational coordination, and collaboration with global research teams.
You will work closely with sponsors, investigative sites, legal teams, and clinical operations professionals to support successful study execution.
This is an ideal opportunity for a detail-oriented professional who thrives in a regulated, collaborative, and mission-driven environment.
Your work will directly contribute to bringing new therapies and medical innovations to patients worldwide.

The Sr. Site Contract and Payment Associate is responsible for managing clinical trial agreements, budgets, and site payment operations while ensuring accuracy, compliance, and operational efficiency throughout the study lifecycle. This role requires strong collaboration across internal teams, sponsors, investigative sites, and legal partners to support successful clinical research delivery.

• Independently facilitate the review, negotiation, and execution of Clinical Trial Agreements (CTAs) and contract amendments with sponsors, sites, and legal stakeholders.
• Develop, review, and negotiate clinical trial budgets, including per-patient costs, start-up fees, pass-through expenses, and overhead considerations.
• Track contract milestones, renewals, amendments, approvals, and payment terms throughout the duration of clinical studies.
• Analyze study protocols to assess financial impacts and ensure budgets align with fair market value expectations.
• Prepare reports and updates related to contract status, budget approvals, and payment progress for project teams.
• Collaborate with cross-functional teams including project management, clinical operations, information technology, and legal teams to resolve operational challenges.
• Manage clinical trial site payments by validating payment triggers, calculating milestones, reconciling invoices, and ensuring accurate and timely processing.
• Monitor data integrations between clinical trial systems and payment platforms, identifying and resolving issues that may impact payment timelines.
• Investigate and resolve payment discrepancies, including overpayments, underpayments, and documentation gaps.
• Provide guidance and support to other team members on contract, budget, and payment processes when needed.
• Maintain compliance with quality standards, regulatory requirements, data integrity practices, and organizational procedures.

The ideal candidate brings experience in clinical research administration, contract management, and payment operations, with strong analytical abilities and excellent attention to detail. Success in this role requires the ability to manage multiple priorities, communicate effectively with diverse stakeholders, and operate within a highly regulated environment.

• Associate’s or Bachelor’s degree in business, life sciences, or a related field, or equivalent combination of education, training, and experience.
• 2+ years of experience in clinical research administration, contract management, budget negotiation, or related functions.
• Experience working with clinical trial agreements, research billing processes, and clinical site payments.
• Background in a clinical research site, contract research organization (CRO), or similar healthcare research environment preferred.
• Strong understanding of clinical trial operations and relevant regulations, including GCP/GxP/ICH guidelines.
• Experience developing, reviewing, and negotiating clinical trial budgets and analyzing study costs.
• Strong organizational skills with the ability to manage multiple studies and deadlines simultaneously.
• Advanced proficiency with Microsoft Excel, Word, Outlook, and related business tools.
• Experience with clinical trial management systems, payment platforms, Veeva Vault, EDC systems, or similar technologies preferred.
• Excellent written and verbal communication skills with the ability to collaborate effectively across teams.
• Analytical mindset with strong problem-solving skills and a commitment to producing accurate, high-quality work.
• Ability to work independently, take ownership, and adapt to changing business needs.
• Demonstrated alignment with values focused on collaboration, operational excellence, scientific rigor, and continuous improvement.

• Competitive salary package based on experience and qualifications.
• Comprehensive medical, dental, and vision coverage beginning on the first day of employment.
• Flexible paid time off, unlimited sick time, and company-paid holidays.
• 401(k) retirement plan through Fidelity with company matching contributions.
• Paid parental leave and family support programs, including adoption and fertility assistance.
• Company-paid life and disability insurance coverage.
• Remote work flexibility with wellness and workspace reimbursement support.
• Employee Assistance Program supporting personal and professional well-being.
• Career development opportunities and opportunities to grow within a global organization.
• Opportunity to contribute to research programs that advance innovative therapies and improve patient outcomes worldwide.