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Syneos Health

Site Contracts Specialist – Senior

Syneos Health

. Negotiate, draft, review, and finalize Clinical Trial Agreements (CTAs) and other site-related contracts for clinical research studies .

Posted 9/24/2026full-timeMorrisville • North Carolina • United StatesSenior💰 $56,400 - $115,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in negotiating and managing Clinical Trial Agreements (CTAs) and site-related contracts, with a strong understanding of the clinical development process and regulatory compliance. Proven ability to mentor junior staff and contribute to training and quality assurance initiatives.

Highest-signal resume keywords
Clinical Trial Agreement NegotiationClinical Development Process KnowledgeProject Management ExperienceExcellent Written/Oral CommunicationVendor Management Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial AgreementsContract NegotiationBudget ManagementRegulatory ComplianceClinical ProtocolsQuality AssuranceProblem-SolvingProject ManagementContract ReviewRisk Identification
Soft Skills
MentoringInterpersonal SkillsTeam OrientationOrganizational SkillsFlexibility
Tools & Technologies
Microsoft Office Suite
Industry Keywords
Clinical ResearchCROPharmaceuticalBiotechnologyICH GCPStudy Start-UpRegulatory AffairsInvestigative SitesAcademic Medical CenterHealthcare Systems

About the role

Key responsibilities & impact
  • Negotiate, draft, review, and finalize Clinical Trial Agreements (CTAs) and other site-related contracts for clinical research studies
  • Lead contract negotiations with investigative sites, hospitals, academic institutions, site networks, and healthcare systems
  • Review legal and commercial terms, including confidentiality, indemnification, insurance, intellectual property, publication rights, and payment provisions
  • Negotiate site budgets and payment schedules with study teams and site representatives
  • Identify contractual risks and propose solutions aligned with company and sponsor requirements
  • Manage contract amendments resulting from protocol changes, study extensions, enrollment adjustments, or budget updates
  • Serve as the primary point of contact for site contract communications with sponsors, sites, legal counsel, and internal stakeholders
  • Mentor, lead, and motivate more junior staff
  • Provide quality feedback and guidance to peers
  • Contribute to training and Quality assurance plans within SSU and update SOPs/WI

Requirements

What you’ll need
  • BA/BS degree in Science, Clinical Research, Medicine, Biology or equivalent combination of education and experience; advanced degree preferred
  • 2+ years of experience negotiating, reviewing, and executing Clinical Trial Agreements (CTAs) and other site-related contracts
  • Experience with a CRO, pharmaceutical/biotechnology sponsor, academic medical center, hospital system, research institution, or investigative site involved in clinical research contracts
  • Strong knowledge of the clinical development process and legal and contracting parameters
  • Strong computer skills in Microsoft Office Suite
  • Ability to manage challenging priorities and remain flexible and adaptable in stressful situations
  • Excellent understanding of clinical trial processes across Phases II-IV and ICH GCP
  • Good understanding of clinical protocols and associated study specifications
  • Excellent understanding of clinical trial start-up processes
  • Project management experience in a fast-paced environment
  • Good vendor management skills
  • Excellent written/oral communication, presentation, documentation, interpersonal, and team-orientation skills
  • Strong organizational skills and ability to handle multiple projects
  • Strong negotiating and problem-solving skills
  • Ability to mentor, lead, and motivate more junior staff
  • Ability to provide quality feedback and guidance to peers
  • Ability to contribute to a training and Quality assurance plan within SSU and update SOPs/WI
  • Experience collaborating with Legal, Clinical Operations, Study Start-Up, Regulatory Affairs, and Finance teams

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • Inclusive workplace culture
  • Company car or car allowance
  • Medical, Dental and Vision health benefits
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO)
  • Sick time