Monitors and manages clinical trial sites from startup through closeout, conducting site visits, training teams, reviewing source data, ensuring protocol and ICH-GCP compliance, supporting audit readiness, and resolving site-level issues. Collaborates with sponsors, vendors, and cross-functional teams while traveling to investigator sites as needed. Requires clinical monitoring experience, relevant education, strong communication skills, language fluency, and a valid driver’s license.
Join Fortrea and play a key role in advancing clinical research while ensuring the highest standards of patient safety and data quality. This is a client-dedicated Unblinded CRA I role, supporting clinical trials where access to treatment assignment information is required.
What you'll do:
- Monitor and manage clinical trial sites from start-up through closeout.
- Conduct site visits, training, and ongoing support for study teams.
- Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
- Review source data and documentation to ensure accuracy and quality.
- Support audit readiness and issue resolution at site level.
- Collaborate with sponsors, vendors, and cross-functional teams to keep studies on track.
- Travel to investigator sites as required.
What we're looking for:
- Degree in Life Sciences, Nursing, or a related field (or equivalent experience).
- At least 6 months of independent monitoring experience.
- Understanding of clinical trial processes and regulatory requirements.
- Strong organizational, communication, and problem-solving skills.
- Fluent English and local language skills.
- Valid driver's license and willingness to travel.
This is a great opportunity to develop your CRA career while contributing to clinical studies that make a difference to patients worldwide!
Learn more about our EEO & Accommodations request here.
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