Senior Site Contracts Lead – Remote US

Syneos Health, Inc.

Maryland

Remote

USD 80,000 - 140,000

Full time

4 days ago
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Benefits offered by this job

Health benefits
401k with company match
Employee Stock Purchase Plan

Job summary

Syneos Health, Inc. is seeking a Senior Site Contracts Manager to develop, negotiate, and manage US site budgets and clinical trial agreements for sponsor-dedicated studies.

You will collaborate with internal teams and major academic institutions to craft robust contracts while minimizing risk. This role requires a strong communicator, leader, and negotiator with experience across multiple therapeutic areas; oncology experience is strongly preferred.

Qualifications

  • 4+ years building budgets and contracts from templates.
  • Direct experience negotiating with large academic institutions.
  • Ability to juggle priorities, lead projects, and deliver results under tight timelines.
  • Strong understanding of clinical study protocols, timelines, and site milestones (e.g., SIV).

Responsibilities

  • Budgeting & Template Development: Build US site budget templates and study-specific budget language.
  • Contract Negotiation & Risk Management: Lead direct negotiations with large academic institutions; draft and finalize CTAs balancing objectives and protections; conduct due diligence checks (FMV, site justification).
  • Project Leadership & Delivery: Prioritize and lead multiple contracting projects across several therapeutic areas (oncology preferred).
  • Tools, Systems & Communication: Proficiency in Excel and CTMS; maintain trackers and communicate updates.
  • Compliance, Collaboration & Continuous Improvement: Deepen knowledge of GCP and sponsor processes; support team Training and process improvements.

Skills

Budgeting
Negotiation
Project management
Communication

Education

Bachelor's degree

Tools

Excel
CTMS (Clinical Trial Management System)

Job description

Syneos Health, Inc. is seeking a Senior Site Contracts Manager to develop, negotiate, and manage US site budgets and clinical trial agreements for sponsor-dedicated studies.

You will collaborate with internal teams and major academic institutions to craft robust contracts while minimizing risk. This role requires a strong communicator, leader, and negotiator with experience across multiple therapeutic areas; oncology experience is strongly preferred.

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