Clinical Research Associate

We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.

Responsibilities:

• Conduct site management and monitoring responsibilities for clinical trials
• Verify study training records and ensure site regulatory documents are complete and current
• Safeguard data integrity through source document review and verification
• Ensure the protection of subjects and adherence to regulatory requirements
• Prepare and implement project plans related to Clinical Monitoring responsibilities
• Travel to study sites and perform on-site monitoring activities
• Work closely with the study team to ensure study deliverables are met

Requirements:

• University or college degree in a related allied health profession (e.g., nursing licensure)
• 2+ years of Clinical Monitoring experience
• Thorough understanding of ICH GCP Guidelines and local regulatory requirements
• Fluent in local office language and English

Preferred Qualifications:

• Thorough working knowledge of Fortrea SOPs for site monitoring
• Additional years of experience in a related field (e.g., medical, clinical, pharmaceutical)
• Phase I monitoring experience
• Life Science or Nursing qualification
• Good computer literacy with working knowledge of PCs, Windows, and Microsoft Office applications