Senior Clinical Contracts Manager

Precision Medicine Group

North (SC)

On-site

USD 111,000 - 166,000

Full time

17 hours ago
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Benefits offered by this job

Health insurance
Retirement savings benefits
Life insurance and disability benefits
Parental leave
Paid time off

Job summary

Precision Medicine Group in South Carolina seeks a Senior Contracts Manager to draft, negotiate and manage site contracts and amendments, ensuring alignment with study timelines. You will work with Clinical Operations teams and serve as a subject matter expert in contract management.

The role requires 7+ years in Clinical Trial/Vendor contracting, strong negotiation and MS Office skills, and the ability to lead interactions across US, Europe and APAC regions.

Qualifications

  • Experience drafting, reviewing and negotiating site Clinical Trial Agreements and vendor contracts.
  • Leading interactions with US/European/APAC institutions and sponsor teams.
  • Detail‑oriented with strong organizational and communication skills.

Responsibilities

  • Review, draft, negotiate and track site contracts and NDAs.
  • Establish processes for overall site contract management.
  • Escalate complex issues with clients and internal stakeholders.
  • Provide guidance on contract terms and operational implications.
  • Maintain contract files and update study teams on status.
  • Mentor new SCMs and Precision for Medicine staff.

Skills

Organizational skills
Written communication
Time management
Professionalism
Independent work
Relationship building
Teamwork in virtual environment
MS Office proficiency

Education

Bachelor's in law or equivalent
Equivalent experience in scientific/healthcare discipline

Tools

MS Office

Job description

Precision Medicine Group in South Carolina seeks a Senior Contracts Manager to draft, negotiate and manage site contracts and amendments, ensuring alignment with study timelines. You will work with Clinical Operations teams and serve as a subject matter expert in contract management.

The role requires 7+ years in Clinical Trial/Vendor contracting, strong negotiation and MS Office skills, and the ability to lead interactions across US, Europe and APAC regions.

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