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Fortrea

Clinical Research Associate II - FSP Team - Portugal

Oeiras

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hirly's read of this role

Role family
Healthcare
Seniority
Mid level
Country
PT
Work mode
On-site / unstated
First seen by hirly
6 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Main Responsibilities:

  • Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
  • Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
  • Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
  • Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
  • Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
  • Ensures audit readiness at site level.

Qualifications (Minimum Required):

  • 2 years minimum of experience as independent monitor with centers in Portugal, specifically in oncology studies.
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
  • Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.
  • Fluent in local office language and in English, both written and verbal.

If you're looking to grow your career within a global organization while working in a collaborative FSP environment, we'd love to hear from you. At Fortrea, you'll have the opportunity to contribute to meaningful clinical research, work alongside industry-leading experts, and help bring innovative therapies to patients worldwide.

Apply today and join Fortrea's FSP team in Portugal, where your expertise can make a real difference in advancing healthcare!

Learn more about our EEO & Accommodations request here .

Original posting on Fortrea's site ↗

Listed on hirly, a job board. hirly is not the employer: Fortrea is hiring for this role.

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