
The Site Contracts & Budget Manager provides operational leadership for site contracting and budget
negotiation activities across awarded clinical trials. The role is primarily accountable for contracting strategy,
Clinical Trial Agreement negotiation and execution, site budget negotiations, amendments, and resolution of
complex contractual and financial issues.
Working in close partnership with the Site Budget & Proposal Manager, the role translates proposal-stage
budget assumptions into effective study- and site-level contracting and negotiation strategies. Together, the
roles provide complementary leadership across the site budget and contracting lifecycle, with distinct primary
areas of accountability.
The Site Contracts & Budget Manager serves as a key contact and escalation point for sponsors, sites, and
internal stakeholders and provides functional guidance, training, and support to Site Budget & Contracting
personnel
More specifically, the Site Contracts and Budget Manager must:
· Lead and manage Site Budget & Contracting staff, providing direction, coaching, development,
workload oversight, and support to ensure consistent quality and delivery across assigned studies.
· Oversee site contracting and budget negotiation activities across the portfolio, ensuring appropriate
resourcing, prioritization, quality, timelines, and escalation of risks or issues.
· Provide oversight of site contracting for awarded clinical trials, including Clinical Trial Agreements,
associated financial exhibits, amendments, negotiation parameters, and country-specific requirements.
· Establish and maintain contracting strategies, standards, and negotiation approaches that support
timely site activation while balancing sponsor requirements, organizational standards, site
expectations, and contractual risk.
· Serve as functional escalation point for complex or high-risk contract and budget negotiations,
providing guidance to team members and facilitating decisions with sponsors, sites, Legal Affairs, and
other stakeholders.
· Oversee the operational implementation of study-specific site budgets, including negotiation
parameters, approval pathways, exceptions, and escalation requirements.
· Translate proposal-stage budget assumptions into executable study- and site-level budget and contracting strategies.
· Collaborate with Legal Affairs, Project Management, Study Start-Up, Regulatory Affairs, Clinical Operations, Finance, and other stakeholders to ensure contracting and budget activities align with study requirements and operational plans.
Profile
At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability, and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
In this position, you will be eligible for the following perks:
Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.
Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Indero: Your Dual-Focus CRO for Dermatology & Rheumatology
At Indero, we specialize in providing comprehensive Contract Research Organization (CRO) services for dermatology and rheumatology. Our team feels like an extension of your own, offering scientific guidance, accurate results, and exceptional customer satisfaction.
Our Expertise: With over 25 years of deep medical and operational expertise in dermatology, we seamlessly translate our knowledge to rheumatology. We understand that dermatology and rheumatology are inextricably linked, as immune-mediated inflammatory skin and joint diseases often require similar treatments.
Our Services: We set the standard with our value-added services, including:
• Study Design and Protocol Development
• Regulatory Submissions and Consulting
• Trial Master Files Management
• Project Management
• Investigator/Site Selection
• Patient Recruitment
• Clinical and Medical Monitoring
• Pharmacovigilance
• Data Management and Biostatistical Analysis
• Clinical Study Reports and Medical Writing
Since 2000, Indero has built a strong reputation for the quality of our research and the care we offer to study participants, clients, and sites. We often exceed our clients' timeline expectations, ensuring successful outcomes for every project.