Unblinded Clinical Research Associate I

About the Role

Become part of Fortrea and contribute significantly to clinical research efforts by ensuring patient safety and high-quality data management. This Unblinded Clinical Research Associate I position is dedicated to clients who require access to treatment assignment details during clinical trials.

Responsibilities

• Oversee and manage clinical trial sites from initiation through to completion.
• Conduct site visits, provide training, and offer continuous support to study teams.
• Ensure adherence to clinical trial protocols, ICH-GCP standards, and all regulatory mandates.
• Perform detailed reviews of source documents and data to confirm accuracy and integrity.
• Assist in preparing sites for audits and resolving any issues at the site level.
• Work closely with sponsors, vendors, and various teams to maintain study progress.
• Travel to clinical investigator sites as necessary.

Candidate Requirements

• A degree in Life Sciences, Nursing, or a similar discipline, or equivalent practical experience.
• At least six months of experience independently monitoring clinical trial sites.
• Solid understanding of clinical trial procedures and regulatory frameworks.
• Excellent organizational, communication, and problem-solving abilities.
• Proficiency in English and local language communication.
• Possession of a valid driver's license and openness to travel for site visits.

Additional Information

This position offers a valuable chance to advance your career as a CRA while impacting patient lives globally through meaningful clinical research. Fortrea is committed to equal employment opportunities and accommodates accommodation requests as appropriate.