[Hiring] Clinical Research Associate (CRA I/II) @Fortrea

Role Description

Fortrea is looking for Clinical Research Associates (CRAs) in Portugal to support early-phase (Phase I) clinical trials, offering the opportunity to work on innovative, first-in-human studies in a dynamic environment.

• Clinical site monitoring: conducts routine, pre‑study, initiation, and close‑out visits, ensuring full compliance with project plans.
• Site and patient protection: ensures informed consent, protocol adherence, and regulatory compliance to safeguard study participants.
• Data quality oversight: performs source document verification, CRF review, and manages data queries to ensure accuracy and completeness.
• Operational site management: prepares trip reports, ensures audit readiness, manages study files, coordinates with vendors, and uses resources efficiently.
• Safety reporting: tracks and follows up on Serious Adverse Events (SAEs), supporting report and narrative preparation.
• Extended support activities: feasibility assessments, QC visits, EC submissions, budget support, training/mentoring of new staff, and local project coordination.
• Cross‑functional communication & logistics: liaises with internal teams, manages study materials, and travels as required.

Qualifications

• University Master's degree in healthcare or similar.
• Basic understanding of the clinical trial process and foundational knowledge of applicable regulatory guidelines.
• Fluency in both English and the local office language, in written and verbal communication.

Requirements

• Mandatory 2 year minimum of experience as CRA.
• Mandatory experience in Phase I trials.
• Understanding of Regulatory Guidelines.
• Good computer skills with good working knowledge of a range of computer packages.

Benefits

• Join a highly collaborative, supportive, and growth‑oriented environment.
• Your development is valued and your contributions truly make an impact.