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From the employer's careers site First seen 3 Nov 2026

Site Contracts Lead

Syneos Health ROU-Remote Remote senior full-time

The employer hasn't listed a salary.

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Description

Syneos Health is seeking a Site Contracts Lead to manage negotiation of clinical study agreements on a study level and drive CTA document finalization and execution.

The successful candidate will oversee negotiations of clinical study agreements, provide oversight of contact and budget negotiations status, and act as a first-line subject matter expert for all CTA elements on assigned studies.

Responsibilities:

  • Oversees negotiations of clinical study agreements on a study level and drives CTA document finalization and execution
  • Provides oversight of contact and budget negotiations status and manages escalation of out-of-parameter queries
  • Acts as first-line subject matter expert for all CTA elements on assigned studies
  • Plans contract execution strategy for assigned studies and coordinates with internal study team stakeholders
  • Coordinates communications between study team stakeholders and global team of site-facing site contract and budget negotiators
  • Works closely with internal stakeholders and with Sponsor to prepare site contractual templates
  • Establishes strong working relationships and collaboration with Sponsor to ensure site contractual templates fit into the global strategy set for the program
  • Creates and maintains document status reports and updates department tools/systems and team members on a regular basis
  • Collaborates with internal and external legal, finance and clinical operations departments
  • Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms
  • May support BU and organization through help desk and other defined pathways to resolve and deescalate issues
  • Performs other work-related duties as assigned

Requirements:

  • 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
  • Thorough knowledge of applicable regulations, drug development and clinical project management procedures
  • Good presentation, documentation and interpersonal skills
  • Proficient in MS Office, MS Project, outlook and Internet
  • Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment
  • Attention to detail, effective oral/written communication skills along with the ability to work independently to meet deadlines

Skills

Required

  • MS Office
  • MS Project
  • clinical trial expertise
  • regulatory knowledge

Nice to have

  • CRO/pharmaceutical industry experience
  • study coordinator experience
  • CRA experience

Ready to apply?

You apply with the employer directly. Their original posting is here: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Remote/Site-Contracts-Lead_25113511-1

Apply on Syneos Health