About the 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
- Preferably 1+ year experience in oncology studies
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
Additional Information
- Willingness to travel (~60% to study sites)
Learn more about our EEO & Accommodations request here.
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