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Site Contract Manager

0-2 years
$62,800 – $157,100
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Site Contract Manager

📍 Location: Durham, North Carolina (Home-based; available in additional locations)
🕒 Employment Type: Full-time
🔖 Job ID: R1503651

Job Overview

Develop and implement global contracting strategies while supporting all required start-up contracting activities for selected sponsors, studies, or multi-protocol programs, as per sponsor requirements.

Essential Functions

Contract Development & Strategy

Coordinate investigator grants, estimates, and proposal text to support proposals.

Develop contract language, payment terms, and budget templates.

Maintain and utilize contracting systems, tools, processes, and training materials.

Collaboration & Communication

Engage with sponsors, stakeholders, and RSU regions/countries to ensure timely delivery of project scope.

Provide specialist legal, operational, and financial support for study teams.

Contribute to creation/review of scientific, technical, and administrative documents.

Contracting Intelligence & Efficiency

Collect, analyze, and disseminate contracting intelligence to support studies.

Ensure adherence to timelines, financial goals, and contracting performance metrics.

Report out-of-scope contracting activities as required.

Quality & Compliance

Collaborate with Quality Management to ensure compliance with contract management standards.

Maintain internal systems such as CTMS, databases, and tracking tools.

Leadership & Mentoring

Mentor and coach colleagues; deliver training materials as needed.

Deliver presentations to clients when required.

Foster long-term client relationships.

Qualifications

Education:

Bachelor’s Degree in a related field (Required).

Equivalent combination of education, training, and experience may be considered.

Experience:

2+ years of relevant sponsor or CRO clinical site contracting experience.

Global/regional contract negotiation experience preferred.

Skills:

Strong negotiating, communication, and interpersonal skills.

Legal, financial, and technical writing proficiency.

Knowledge of clinical trial regulations, GCP/ICH, and drug development processes.

Strong organizational, planning, and presentation skills.

Proficient in Microsoft Office and email applications.

Ability to lead, motivate, coach, and mentor.

Effective in matrix team environments and relationship building.

Compensation & Benefits

💰 Base Pay Range (Annualized): $62,800 – $157,100

Actual pay depends on knowledge, skills, education, experience, and location.

Incentive plans, bonuses, health, welfare, and additional benefits may be offered.

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. We accelerate the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.

🌐 Learn more: https://jobs.iqvia.com