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Site Budget & Contract Lead - Sponsor dedicated

Role overview

Qualifications

  • BS degree or international equivalent
  • 4 or more years of experience in clinical research site contracting and budgeting
  • At least 2 years of site budgeting and contracting oversight
  • Fluency in local language and English

Responsibilities

  • Manage escalations and review of assigned site budgets and contracts
  • Support the development of processes, methodologies, data, and technologies for service delivery improvements
  • Develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets
  • Manage site contracts and budgets negotiation timelines to ensure sites are 'Ready To Enroll'

Key facts

Other skills

  • Budgeting
  • Decision Making
  • Communication

About the company

Fortrea logo

Fortrea

Contract Research Organizations (CRO)

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

Site Budget & Contract Lead (Full-Time, Permanent, Remote) - Sponsor dedicated

We are currently seeking an experienced Site Budget & Contract Lead to join our team in a full-time, permanent, remote position. This is an exciting opportunity for a clinical research professional who enjoys leading site budgeting and contracting activities while playing a key role in accelerating study startup timelines.

Role objectives

  • Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.

  • Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the service delivery

Responsibilities:

  • Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.

  • Oversight of assigned country budget setup including parameters development.

  • Partner with Study Startup, SB&C team and Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.

  • Leverage leading industry tools and data sources to provide budget and contract feedback aligned with company parameters and fair market value guidance.

  • Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.

  • Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.

Requirements:

  • BS degree or international equivalent

  • 4 or more years of experience in clinical research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.

  • At least 2 years of site budgeting and contracting oversight

  • Ability to explain data, facilitate decision making processes to be data driven.

  • Expertise in principles driving country/site budgeting and contracting strategies.

  • Excellent organizational skills, decision making, communication and negotiation skills.

  • Fluency in local language and English

Learn more about our EEO & Accommodations request here.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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