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CRA II

Role overview

Qualifications

  • Monitoring experience in clinical trials
  • Curiosity and comfort with complexity
  • Strong communication and stakeholder skills
  • A desire to grow your portfolio and your career

Responsibilities

  • Lead and manage sites across varied and complex indications
  • Build trusted relationships with investigators and study teams
  • Ensure patient safety and data integrity remain paramount
  • Contribute actively to innovative and first-in-class studies

Key facts

  • Remote from: United Kingdom, Mexico
  • Full time
  • Mid-level (2-5 years)
  • English

Other skills

  • Communication
  • Teamwork
  • Curiosity
  • Relationship Building

About the company

Fortrea logo

Fortrea

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
Industry
Company size10001

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Job description


Work Across Cutting‑Edge Science That Truly Makes a Difference

What if your CRA role exposed you to some of the most exciting and meaningful science in clinical research?
 

At Fortrea, our CRAs don’t sit in narrow silos. You’ll work across a diverse and challenging portfolio that reflects where medicine is going, not where it’s been.
 

Our study portfolio includes:

🧬 Oncology
🧠 Neuroscience
💊 General Medicine
🧫 Cell & Gene Therapy
🧬 CAR‑T Therapy Studies
 

This means real complexity, real learning, and the chance to build a profile that sets you apart as a CRA.
 

Why CRAs choose us:

Breadth of experience – develop expertise across multiple therapeutic areas
Exposure to advanced therapies – cell & gene, CAR‑T, innovative trial designs
Supportive leadership – managers who understand the demands of complex studies
Career acceleration – skills that open doors, not limit them
A culture of trust – autonomy, collaboration, and respect for your expertise
 

If you’re a CRA who enjoys scientific challenge, values quality over box‑ticking, and wants to feel proud of the studies you support - this could be your next move!
 

The role:

  • Lead and manage sites across varied and complex indications

  • Build trusted relationships with investigators and study teams

  • Ensure patient safety and data integrity remain paramount

  • Contribute actively to innovative and first‑in‑class studies
     

We’re looking for:

✅ Monitoring experience in clinical trials
✅ Curiosity and comfort with complexity
✅ Strong communication and stakeholder skills
✅ A desire to grow your portfolio and your career

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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