FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Site Contracts Specialist – LATAM Experience
Syneos HealthSite Contracts Specialist managing clinical trial agreements, budgets, and negotiations for Syneos Health, a global life sciences services organization, in Argentina. Supporting site start-up and multi-country studies.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in contract management processes, including negotiation, preparation, and execution of clinical trial agreements. Proficient in project management, vendor management, and compliance with clinical trial protocols and regulations.
Highest-signal resume keywords
Contract Management ExperienceClinical Trial Processes KnowledgeProject Management ExperienceNegotiation SkillsVendor Management Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Contract NegotiationBudget PreparationQuality ControlClinical Trial DocumentationSOP ComplianceMetadata CaptureClinical Protocol ReviewContract Management DocumentationSSU Tracking SystemTraining and Mentoring
Soft Skills
Excellent Communication SkillsOrganizational SkillsProblem-Solving SkillsTeam OrientationFlexibility and Adaptability
Tools & Technologies
Microsoft Office SuiteSSU Tracking System
Industry Keywords
Clinical Development ProcessContract Research OrganizationPharmaceutical IndustryICH GCPClinical Trial Start-Up Processes
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Administer contract management processes for protocol, informed consent, institution, investigator, vendor, consultant, and customer agreements at project level
- Lead or support multi-country clinical trial contracting, including negotiating and preparing contracts, budgets, and related documents
- Support country template contract and budget agreements and produce site-specific contracts
- Submit proposed contracts and budgets for sites and negotiate issues with sites, sponsors, and internal teams
- Perform quality control, arrange execution of clinical trial agreements, archive documents, and capture metadata
- Review contracts for completeness and accuracy and document corrections
- Support business development and represent site contracts/Site Start-Up at internal or customer meetings
- Project-manage ongoing contract issues and follow up on outstanding items
- Generate amended contracts and budgets, prepare contract management documentation, and streamline processes
- Track country/site contracting timelines and milestone progress in the SSU tracking system
- Collaborate with legal, finance, clinical operations, vendors, sponsors, and other internal and external stakeholders
- Facilitate contract execution by company signatories
- Maintain contract templates, site-specific files, databases, training materials, and training records
- Train and mentor less experienced staff and provide functional guidance and feedback
- Act as communication liaison regarding contract statuses and pending issues
- Monitor project financial aspects and contracted hours/tasks and escalate discrepancies
- Review and comply with SOPs and Work Instructions and ensure timesheet compliance
- Contribute to SSU training and quality assurance plans and update SOPs/WIs
Requirements
What you’ll need- BA/BS degree in Business Administration, Public Administration, Public Health, related field, or equivalent combination of education and experience
- Advanced degree preferred
- High level of contracts management experience
- Experience in a contract research organization or pharmaceutical industry essential
- 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 and oral communication, presentation, documentation, and interpersonal skills
- Strong team orientation and organizational skills
- Proven ability to handle multiple projects
- Quality-driven approach
- 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 training and quality assurance plans within SSU and update SOPs/WIs
Benefits
Comp & perks- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition
- Total rewards program
- Inclusive culture
- Comprehensive resources including emerging technologies, data, science and knowledge sharing
- Career paths and employment opportunities
- Reasonable accommodations, when appropriate