Site Contracts Lead

Syneos Health

. Oversee negotiations of clinical study agreements at study level .

Posted 10/27/2026full-timeRemote • Taiwan, ChinaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study agreement negotiations, contract execution strategies, and stakeholder communication. Proficient in managing budgets and timelines while ensuring compliance with applicable regulations and clinical project management procedures.

Highest-signal resume keywords

Clinical Study Agreement NegotiationContract Execution StrategyBudget ManagementStakeholder CommunicationRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ExpertiseContractual Language ProficiencyFinancial Attachment ManagementInvestigator Grant BudgetingDocument Status Reporting

Soft Skills

Interpersonal SkillsEffective CommunicationLeadership SkillsAttention to DetailAbility to Work Independently

Tools & Technologies

MS OfficeMS ProjectOutlookInternet

Industry Keywords

CROPharmaceutical IndustryClinical Project ManagementStudy CoordinatorHealthcare Administration

About the role

Key responsibilities & impact

Oversee negotiations of clinical study agreements at study level
Drive CTA document finalization and execution, including contractual language and terms, financial attachments, and investigator grant budgets
Provide oversight of contract and budget negotiation status
Manage escalation of out-of-parameter budgetary and contractual requests to sponsor decision-makers
Act as first-line subject matter expert for CTA elements on assigned studies
Advise stakeholders on issue resolution
Plan contract execution strategy and forecast site-specific contractual execution timelines
Coordinate CTA strategy with internal study team stakeholders and overall study start-up plans
Manage expectations of internal and sponsor study teams regarding global CTA negotiations
Coordinate communications between study stakeholders and global site contract and budget negotiators
Participate in regular study calls
Prepare site contractual templates, payment terms, study-level negotiation parameters and processes
Collaborate with sponsors to align site contractual templates with global program strategy
Create and maintain document status reports and update department tools, systems, and team members
Maintain appropriate documentation
Collaborate with legal, finance, and clinical operations departments
Manage discussions regarding fair market value of investigator budgets and payment terms
Support business units and the organization through help desk and other defined pathways
Perform other work-related duties as assigned

Requirements

What you’ll need

BS degree in life sciences, a health related field, or equivalent combination of education and experience
Preferred experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience
Thorough knowledge of applicable regulations, drug development and clinical project management procedures
Good presentation, documentation and interpersonal skills
Proficient in MS Office (Word, Excel and PowerPoint), MS Project, Outlook and Internet
Ability to handle multiple tasks and meet deadlines in a dynamic environment
Attention to detail
Effective oral and written communication skills
Ability to work independently to meet deadlines
Strong leadership skills
Ability to teach and mentor team members
Minimal travel may be required, up to 25%

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition
Total rewards program
Inclusive culture
Reasonable accommodations when appropriate