Site Contracts Lead

ICON Clinical Research

Santiago

Hybrid

CLP 9,000,000 - 15,000,000

Full time

33 hours ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Annual leave entitlements
Health insurance
Retirement planning offerings
Global Employee Assistance Programme (
Life assurance
Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Chile is seeking a Site Contracts Lead to oversee contract management for clinical trial agreements and budgets. You will coordinate end-to-end contracting activities, negotiate terms, and ensure timely delivery while balancing sponsor, site, and internal requirements.

You will guide a team of Site Contracts Negotiators, drive process improvements, and collaborate closely with legal, finance, and project teams to align on language, budgets, and risk positions.

Qualifications

  • Bachelor's degree or equivalent experience in law, business, life sciences, or related field.
  • Strong experience in clinical site contracting or similar contract negotiation roles within CRO, pharma, or healthcare.
  • Good understanding of clinical trial agreements, budget structures, and key legal and compliance considerations.
  • Excellent negotiation, communication, and problem-solving skills.
  • Organised and detail-oriented, with the ability to manage multiple studies and priorities.
  • Collaborative mindset with experience guiding or coordinating the work of others.

Responsibilities

  • Oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations.
  • End-to-end site contracting activities for assigned studies, including template use, negotiation, and execution tracking.
  • Serve as a primary escalation point for contract issues, proposing solutions that balance sponsor, site, and internal requirements.
  • Collaborate with legal, finance, and project teams to ensure alignment on contract language, budget assumptions, and risk positions.
  • Monitor contracting timelines and metrics, identify bottlenecks, and drive corrective actions to improve cycle times.
  • Provide guidance and oversight to Site Contracts Negotiators working on the same studies or programmes.
  • Contribute to the development and refinement of contracting playbooks, templates, and standard processes.

Skills

Contract management
Negotiation
Communication
Problem-solving
Organization

Education

Bachelor's degree in law, business, life sciences, or related field

Job description

COM Finance - Chile - Hybrid

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Site Contracts Lead at ICON, you will oversee and coordinate the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies or portfolios.

What You Will Do:

You will oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:

  • Managing end-to-end site contracting activities for assigned studies, including template use, negotiation, and execution tracking.

  • Serving as a primary escalation point for contract issues, proposing solutions that balance sponsor, site, and internal requirements.

  • Collaborating with legal, finance, and project teams to ensure alignment on contract language, budget assumptions, and risk positions.

  • Monitoring contracting timelines and metrics, identifying bottlenecks, and driving corrective actions to improve cycle times.

  • Providing guidance and oversight to Site Contracts Negotiators working on the same studies or programmes.

  • Contributing to the development and refinement of contracting playbooks, templates, and standard processes.

Your Profile:

You will have solid contract management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience.

  • Strong experience in clinical site contracting or similar contract negotiation roles within CRO, pharma, or healthcare.

  • Good understanding of clinical trial agreements, budget structures, and key legal and compliance considerations.

  • Excellent negotiation, communication, and problem-solving skills.

  • Organised and detail-oriented, with the ability to manage multiple studies and priorities.

  • Collaborative mindset with experience guiding or coordinating the work of others.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Trial Coordinator
Clinical Trial Coordinator

ICON Clinical Research • Santiago

Hybrid
CLP 41,257,000 - 62,868,000
Annual leave entitlements
Health insurance options
Retirement planning
+3
Clinical Operation Manager- Financial
Clinical Operation Manager- Financial

ICON Strategic Solutions • Santiago

Hybrid
CLP 70,313,000 - 107,422,000
Health insurance
Retirement planning
Employee assistance program
+2
Clinical Research Associate
Clinical Research Associate

ICON Clinical Research • Santiago

Remote
CLP 18,000,000 - 24,000,000
Annual leave
Health insurance
Retirement planning
+3
Clinical Research Associate
Clinical Research Associate

ICON Strategic Solutions • Santiago

On-site
CLP 18,000,000 - 28,000,000
Site Contracts Lead — Hybrid Clinical Trials Negotiations
Site Contracts Lead — Hybrid Clinical Trials Negotiations

ICON Clinical Research • Santiago

Hybrid
CLP 9,000,000 - 15,000,000
Annual leave entitlements
Health insurance
Retirement planning offerings
+3
Import Export Associate
Import Export Associate

ICON Clinical Research • Santiago

Remote
CLP 12,000,000 - 24,000,000
Various annual leave entitlements
Health insurance offerings
Retirement planning offerings
+1
Hybrid Clinical Trial Coordinator: Site Monitoring
Hybrid Clinical Trial Coordinator: Site Monitoring

ICON Clinical Research • Santiago

Hybrid
CLP 41,257,000 - 62,868,000
Annual leave entitlements
Health insurance options
Retirement planning
+3
Clinical Research Associate II — Global Trials & Data
Clinical Research Associate II — Global Trials & Data

ICON Clinical Research • Santiago

Remote
CLP 18,000,000 - 24,000,000
Annual leave
Health insurance
Retirement planning
+3
FSP Clinical Trial Coordinator
FSP Clinical Trial Coordinator

ThermoFisher Scientific • Santiago

On-site
CLP 12,000,000 - 18,000,000
CRA II or Sr CRA (sponsor dedicated) - Min 3 years of prev exp in monitoring - Santiago, home-based
CRA II or Sr CRA (sponsor dedicated) - Min 3 years of prev exp in monitoring - Santiago, home-based

7050 INC Research Clinical Services Mexico Limited, S.A. de C.V. • Santiago

Hybrid
CLP 43,732,000 - 72,886,000