Clinical Research Associate (CRA II) – FSO

About the role

As a Clinical Research Associate (CRA II) you will act as the bridge between science and solutions, supporting the delivery of clinical trials across multiple therapeutic areas. You will work under the guidance of experienced colleagues, gaining hands‑on experience in site monitoring, data verification and investigational product management.

Key responsibilities

• Support the management of trial sites in line with Fortrea SOPs, ICH‑GCP, study protocols and sponsor requirements.
• Assist with site initiation, routine monitoring and close‑out visits, ensuring patient safety and protocol compliance.
• Perform source data verification, resolve queries and review eCRFs to maintain data quality.
• Maintain trial documentation in eTMF and sponsor systems to ensure inspection readiness.
• Track investigational product accountability in collaboration with the study team.
• Collaborate with cross‑functional teams, escalating issues to protect site performance, quality and timelines.

Required profile

• University or college degree in life sciences, nursing, pharmacy or a related field.
• Minimum of 2 years of onsite monitoring experience.
• Basic understanding of ICH‑GCP guidelines and clinical trial processes.
• Strong attention to detail, willingness to learn and ability to follow documented procedures.
• Fluency in English, both written and spoken.
• Comfortable using clinical systems and tools; willing to travel for site visits.

Required skills

What we offer

• Structured career development with clear pathways and mentoring.
• Hands‑on exposure to global trials in oncology, dermatology, respiratory, cardiology and diabetes.
• Formal training programs, modern clinical systems and continuous learning opportunities.
• Flexible work model, competitive benefits and a collaborative culture focused on quality and well‑being.