Site Contracts Associate, IQVIA Biotech - UK based
About this opportunity
Site Contracts Associate
IQVIA Biotech
UK - Hybrid in Reading or Paddington
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.
📌 Overview
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 organizational 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.
If you’re passionate about driving excellence in clinical trial contracting and want to make an impact across global programs, we encourage you to apply!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 335 comparable Associate Clinical Development roles across 55 biopharma companies.
Salary context
92 of 335 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 335 comparable roles
+ 33 more countries
Seniority mix
335 of 335 peers have a known seniority level
Therapeutic area mix
20 of 335 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.