Fortrea Logo

Fortrea

CRA II

Reposted 6 Days Ago
Be an Early Applicant
In-Office
Maidenhead, Berkshire, England, GBR
Mid level
In-Office
Maidenhead, Berkshire, England, GBR
Mid level
The CRA II role involves managing complex clinical trial sites, building relationships with investigators, ensuring patient safety, and contributing to innovative studies in various therapeutic areas.
The summary above was generated by AI

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.

Similar Jobs

Yesterday
In-Office
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical
Conducts site qualification, initiation, monitoring, management, and close-out activities for clinical and real-world studies. Ensures regulatory, ICH-GCP, protocol, data integrity, informed consent, investigational product, and documentation compliance. Reviews source records, case report forms, and site files; resolves queries; supports recruitment, audits, training, and investigator meetings. Manages site communications, timelines, action items, and study documentation while collaborating with sponsors, affiliates, medical staff, and local teams. Requires regular travel of up to 75%.
Top Skills: Case Report Forms (Crf)Electronic Data Capture (Edc) SystemsIch-GcpInvestigator Site File (Isf)Trial Master File (Tmf)
Yesterday
In-Office
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical
Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities. Verifies informed consent, source documents, clinical data, investigational product handling, regulatory compliance, and essential trial documentation. Supports recruitment, query resolution, audit readiness, investigator meetings, and site communications. Requires knowledge of GCP and applicable regulations, strong communication skills, computer proficiency, and regular travel of up to 75%.
Top Skills: Case Report Forms (Crfs)Electronic Data Capture (Edc) SystemsIch-GcpInvestigator Site Files (Isfs)Trial Master Files (Tmfs)
Yesterday
In-Office
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical
Conducts clinical trial site qualification, initiation, monitoring, management, and closeout activities. Ensures compliance with protocols, ICH-GCP, regulations, and SOPs; verifies informed consent, source data, case report forms, investigational product handling, and essential documents. Resolves queries, supports recruitment and retention, maintains audit readiness, trains site personnel, documents monitoring activities, and manages site-level timelines and communications. Requires frequent travel to assigned sites.
Top Skills: Electronic Data Capture (Edc) Systems

What you need to know about the London Tech Scene

London isn't just a hub for established businesses; it's also a nursery for innovation. Boasting one of the most recognized fintech ecosystems in Europe, attracting billions in investments each year, London's success has made it a go-to destination for startups looking to make their mark. Top U.K. companies like Hoptin, Moneybox and Marshmallow have already made the city their base — yet fintech is just the beginning. From healthtech to renewable energy to cybersecurity and beyond, the city's startups are breaking new ground across a range of industries.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account