CRA II - Sponsor dedicated

fortrea· FTDEN Fortrea Denmark ApS
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🌍 Remote📍 SoborgFull time

About this role

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.

Frequently Asked Questions

Is the salary disclosed for the CRA II - Sponsor dedicated position at fortrea?
The salary for this CRA II - Sponsor dedicated role at fortrea is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Is the CRA II - Sponsor dedicated job at fortrea remote?
Yes, this CRA II - Sponsor dedicated position at fortrea is remote, with team members based in Soborg. You can work from home or anywhere in the supported regions.
Is the CRA II - Sponsor dedicated role at fortrea full-time or part-time?
This is listed as a Full time position. It is posted as a CRA II - Sponsor dedicated role in the FTDEN Fortrea Denmark ApS department at fortrea.
Which team or department does the CRA II - Sponsor dedicated at fortrea belong to?
This CRA II - Sponsor dedicated position is part of the FTDEN Fortrea Denmark ApS department at fortrea. See the full job description for more information about the team structure and responsibilities.
How do I apply for the CRA II - Sponsor dedicated position at fortrea?
Click the "Apply Now" button on this page. You will be redirected to fortrea's official application portal hosted on workday where you can submit your application directly.
When was the CRA II - Sponsor dedicated job at fortrea posted?
This CRA II - Sponsor dedicated position at fortrea was posted on Aug 5, 2026. Apply as soon as possible — early applications are often reviewed first.
CRA II - Sponsor dedicated
fortrea
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You'll be redirected to fortrea's official application page on Workday.