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Syneos Health

Senior Site Contracts Specialist

Syneos Health

. Lead multi-country projects, including negotiating and preparing contracts, budgets, and related documents for industry-sponsored clinical trials .

Posted 9/22/2026full-timeRemote • United StatesSenior💰 $56,400 - $95,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in contract management and negotiation within the clinical trial landscape, with a strong understanding of the clinical development process and regulatory compliance. Proven ability to manage multi-country projects, mentor junior staff, and ensure quality in all contract-related activities.

Highest-signal resume keywords
Contract ManagementClinical Development ProcessProject ManagementNegotiation SkillsVendor Management

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
Contracts ManagementClinical Trial ProcessBudget ManagementQuality ControlSOP ComplianceMicrosoft Office SuiteClinical ProtocolsProject TrackingTraining DevelopmentRisk Identification
Soft Skills
Excellent CommunicationOrganizational SkillsProblem-Solving SkillsInterpersonal SkillsMentoring Ability
Tools & Technologies
SSU Tracking SystemContract Management Software
Industry Keywords
Clinical TrialsPharmaceutical IndustryContract Research OrganizationICH GCPPhases II-IV

About the role

Key responsibilities & impact
  • Lead multi-country projects, including negotiating and preparing contracts, budgets, and related documents for industry-sponsored clinical trials
  • Produce and review site-specific contracts from country clinical trial agreement templates
  • Submit proposed CTAs and investigator budgets for site review
  • Negotiate budgets and contracts with sites, Site Contracts Service Centre, SSUL, and sponsors
  • Perform quality control, arrange execution of CTAs, archive documents, and capture metadata
  • Administer contract management processes and coordinate related protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement documents
  • Generate amended contract and budget documents and prepare project contract-management documentation
  • Work with Site Contract Service Center and Legal to harmonize site contracts with sponsor master service agreement terms
  • Collaborate with SSU lead, Clinical Operations, and Finance to validate departmental budgets and backlog
  • Identify contract or process risks and develop solutions; escalate deviations as appropriate
  • Support business development and represent site contracts/SSU at internal or customer meetings
  • Track country/site contracting milestones and comply with forecasted timelines using the SSU tracking system
  • Collaborate with legal, finance, and clinical operations teams on legal and budgetary issues
  • Maintain contract templates, budget templates, site-specific files, and databases
  • Serve as communication liaison regarding contract statuses and pending issues; prepare correspondence
  • Train and mentor less experienced staff and maintain training materials
  • Participate in discussions about company goals, departmental objectives, and project aims
  • Facilitate contract execution by company signatories
  • Monitor project financial aspects and contract hours/tasks; escalate discrepancies
  • Review and comply with SOPs and WIs, update training records, and ensure timesheet compliance

Requirements

What you’ll need
  • BA/BS degree in Business Administration, Public Administration, Public Health, related field, or equivalent combination of education and experience
  • Moderate contracts management experience, including experience in a contract research organization or pharmaceutical industry
  • Strong knowledge of the clinical development process and legal and contracting parameters
  • Strong computer skills in Microsoft Office Suite
  • Excellent understanding of clinical trial process 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
  • Strong organizational skills with proven ability to handle multiple projects
  • Excellent communication, presentation and interpersonal skills
  • Quality-driven in all managed activities
  • Strong negotiating skills
  • Strong problem-solving skills
  • Ability to mentor 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
  • Advanced degree preferred
  • Management experience preferred

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • 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
  • Reasonable accommodations, when appropriate