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Syneos Health

Site Contract Specialist – Sponsor Dedicated

Syneos Health

. Review contract language and budgets for completeness and accuracy, ensuring corrections are made and documented .

Posted 10/6/2026full-timeRemote • North Carolina • United StatesJunior💰 $56,400 - $95,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Clinical Trial Agreements (CTAs), including drafting, negotiation, and lifecycle management, while effectively managing project timelines and stakeholder relationships. Proficient in budget development and negotiation strategies within the clinical trial framework.

Highest-signal resume keywords
Clinical Trial Agreement ManagementBudget Negotiation StrategiesProject Management SkillsStakeholder Relationship BuildingICH-GCP Compliance

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 Agreement DraftingContract Lifecycle ManagementBudget DevelopmentNegotiation DocumentationClinical Trial Start-Up Processes
Soft Skills
Exceptional CommunicationRelationship-Building AbilitiesStrong Organizational SkillsPrioritization SkillsLeadership Experience
Tools & Technologies
Microsoft Office SuiteClinical Trial Tracking Systems
Certifications & Qualifications
SCS-II/Contract Manager 2Senior SCS/Contract Manager 3
Industry Keywords
CRO ExperienceSponsor-Dedicated/FSP ModelPhase II-IV Clinical TrialsProcess Improvement Initiatives

About the role

Key responsibilities & impact
  • Review contract language and budgets for completeness and accuracy, ensuring corrections are made and documented
  • Maintain internal project trackers with accurate and timely information
  • Use sponsor legal fallback language to negotiate site contracting language
  • Negotiate study budgets within approval parameters and follow escalation processes
  • Attend weekly internal and external progress meetings and provide updates and next steps
  • Collaborate with stakeholders to align contract execution dates and site activation timelines
  • Establish and maintain positive relationships with internal and external stakeholders
  • Identify contractual or operational risks and proactively drive solutions
  • Prepare contract and budget escalations
  • Draft and finalize study start-up documents, templates, and start-up plans
  • Prepare and lead study team kick-off meetings
  • Schedule contract and budget preparation and overview meetings
  • Prepare final contracts after negotiations and approvals
  • Participate in pilot and stretch projects aligned with role and sponsor initiatives

Requirements

What you’ll need
  • Bachelor's degree in Business, Public Health, Life Sciences, or a related field, or equivalent experience
  • Demonstrated experience independently managing Clinical Trial Agreements (CTAs), CTA amendments, site budget negotiations, and contract lifecycle management with minimal oversight
  • Strong understanding of CTA drafting and negotiation
  • Knowledge of contract templates and fallback language
  • Knowledge of budget development and negotiation strategies
  • Knowledge of clinical trial start-up processes
  • Experience maintaining negotiation status and documentation within Sponsor or internal clinical trial tracking systems
  • Excellent understanding of Phase II-IV clinical trials, ICH-GCP, and clinical development processes
  • Strong project management, organization, and prioritization skills
  • Exceptional negotiation, communication, and relationship-building abilities
  • Proficiency with Microsoft Office Suite
  • SCS-II/Contract Manager 2: minimum of one year of direct site contract and budget negotiations within a CRO, site, or pharma company required
  • Senior SCS/Contract Manager 3: minimum of two years of direct site contract and budget negotiation required, including at least one year of progressive experience leading site contract negotiations as a client-facing point of contact within an industry-sponsored clinical trial setting
  • Previous Sponsor-Dedicated/FSP model experience preferred
  • Leadership or mentoring experience preferred for senior level
  • CRO experience preferred
  • Experience supporting process improvement initiatives within Site Start-Up or Site Contracts preferred

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 401(k)
  • 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