Jobs Companies Fortrea CRA II - Sponsor dedicated

About this CRA II - Sponsor dedicated role at Fortrea

Fortrea · Onsite · Soborg

Join Fortrea as a CRA – exciting future opportunities for a single sponsor

We’re excited to invite CRAs to join Fortrea, where you’ll work with one dedicated sponsor.

Key requirement:

  • Minimum 2 years of clinical monitoring experience

  • Experience in oncology studies preferred

Summary of Responsibilities

  • Manage clinical trial sites in line with Fortrea SOPs, ICH GCP and sponsor requirements

  • Perform all monitoring visits (PSV, SIV, routine, close-out)

  • Ensure patient safety by verifying informed consent and protocol adherence

  • Maintain data integrity through SDV, query management, and data review

  • Keep site regulatory documentation and eTMF up to date

  • Oversee investigational product handling, storage, and accountability

  • Ensure audit readiness and compliance with quality standards and CRA metrics

  • Prepare monitoring plans, visit reports, and study documentation

On-site Monitoring Responsibilities

  • Ensure site staff are trained and equipped to run the study

  • Verify subject eligibility, consent, and protocol compliance

  • Review source data for accuracy and completeness

  • Identify and resolve data discrepancies and deviations

  • Perform efficient monitoring activities in line with SOPs and travel policy

  • Submit timely and accurate visit reports

  • Track study progress, IP shipments, and serious adverse events

  • Collaborate closely with study teams to meet timelines and deliverables

Additional Responsibilities

  • Support investigator/site management activities

  • Work with CTMS and other eClinical systems

  • Attend investigator meetings and project calls

  • Deliver site training and support onboarding of new team members

  • Contribute to study planning and monitoring strategy

Qualifications & Experience

  • Degree in life sciences or related field (or equivalent experience)

  • Strong knowledge of ICH GCP and clinical trial processes

  • Minimum 2 years of clinical monitoring experience

  • Ability to monitor independently with minimal supervision

  • Experience with SAE reporting and clinical data review

  • Strong organizational, problem-solving, and communication skills

Learn more about our EEO & Accommodations request here.

Ready to apply to Fortrea?
Apply to Fortrea

About Fortrea

At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

See all jobs at Fortrea →

Similar jobs

Sign up for suggestions tailored to the jobs you open and the searches you save.

More jobs at Fortrea

See all jobs at Fortrea →

Apply now
🤖

Whoa — hold up

JobsRadar was built for real people having a rough time in their job search — not for automated requests. You're clicking way too fast and you're now temporarily blocked.

Come back later. If you're genuinely job hunting, we've got your back — just act like a human.

Catch your next role the second it’s posted.

Create a free account and we’ll watch the boards for you — the instant a job matches your search, it lands in your inbox or Telegram. No digging, no refreshing.

Create free account

Free forever · takes 30 seconds · already have one?

Get an edge on your job hunt.

Join our Telegram channel for the stuff that helps you land the role — salary benchmarks, the weekly market pulse, and new-feature drops. No spam, just signal.

Join the channel — it's free