# Site Contracts Associate

**Company**: IQVIA Biotech
**Location**: Reading, Berkshire
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Senior-Site-Contracts-Associate--IQVIA-Biotech---UK_R1566237-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_0c9e5ff3-c8b

## Description

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. Agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.

We are seeking an experienced Site Contracts Associate to manage contract strategy for selected sponsors. In this role, you will support complex studies and multi-protocol programs, ensuring high-quality delivery and operational excellence.

**Key Responsibilities**

- Negotiate clinical trial contracts with research sites, ensuring agreements are completed on time and meet quality and compliance requirements.

- Manage contract changes and additional agreements while balancing business needs and regulatory requirements.

- Support contract planning and study start-up activities for assigned sponsors, studies, and programs.

- Help develop investigator grants, site budgets, contracting plans, and proposal documents.

- Prepare and negotiate contract terms, payment schedules, and budget templates based on project and sponsor needs.

- Work closely with sponsors, stakeholders, and regional study start-up teams to achieve project goals and timelines.

- Provide contract-related guidance and support to study teams on operational and financial matters.

- Gather and share contract and market information to support study planning and decision-making.

- Monitor contract activities to ensure timelines, milestones, and financial goals are met.

**Qualifications & Experience**

- Bachelor’s degree or equivalent.

- 3-5 years of experience in clinical research contract management or a similar role.

- Familiarity with clinical trial processes, regulatory requirements, and contract lifecycle management.

- Strong analytical, organisational, and communication skills.

**What We Offer**

- Opportunity to work on global, high-complexity clinical programs.

- A collaborative, supportive, and growth-oriented environment.

- The chance to influence key clients and shape contracting strategy at scale.

- Career progression and professional development opportunities.

## Skills

### Required
- clinical trial contract management
- regulatory requirements
- contract lifecycle management
- analytical skills
- organisational skills
- communication skills

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Senior-Site-Contracts-Associate--IQVIA-Biotech---UK_R1566237-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)