Manages and monitors clinical trial sites from initiation through closeout, ensuring patient safety, regulatory compliance, protocol adherence, and data integrity. Prepares monitoring reports, maintains study files, supports feasibility and regulatory activities, coordinates vendors and internal teams, and serves as lead monitor. Mentors junior staff and travels extensively to support site activities and audit readiness.
Shape the Future of Clinical Research with Fortrea
At Fortrea, we are redefining the clinical research landscape through innovation, collaboration, and a commitment to improving health worldwide. Join a global team where your expertise drives meaningful impact, and your career growth is supported every step of the way.
About the Role
As a Senior Clinical Research Associate, you will play a pivotal role in ensuring the success of clinical trials by managing and monitoring study sites. You’ll work closely with investigators and sponsors to uphold regulatory standards and deliver high-quality data that advances medical breakthroughs.
Key Responsibilities:
- Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.
- Ensure patient safety and compliance with informed consent and protocol requirements.
- Review source documents and verify data integrity on Case Report Forms (CRFs).
- Prepare accurate and timely monitoring reports and maintain study files.
- Serve as lead monitor for assigned protocols and assist in developing monitoring plans.
- Coordinate with vendors and internal teams to meet project timelines and objectives.
- Support feasibility assessments, budget negotiations, and regulatory submissions.
- Mentor and train junior team members through co-monitoring and guidance.
- Travel extensively (60–80%) to support site activities and maintain audit readiness.
Qualifications
- Bachelor’s degree in life sciences or related field, or equivalent clinical research experience.
- Typically a minimum 3 years of clinical monitoring experience in pharmaceutical or CRO settings.
- Strong knowledge of regulatory requirements and drug development processes.
- Advanced site monitoring and management skills.
- Excellent communication, organizational, and problem-solving abilities.
- Proficiency in relevant computer applications and systems.
- Valid driver’s license and ability to travel extensively.
Why Join Fortrea?
- Global Impact: Contribute to groundbreaking research that improves lives worldwide.
- Career Growth: Access robust training, mentorship, and advancement opportunities.
- Flexibility & Support: Thrive in a collaborative, inclusive environment that values work-life balance.
- Innovation: Be part of a forward-thinking organization shaping the future of clinical trials.
Ready to make a difference? Apply today and be part of a team that’s transforming healthcare.
Learn more about our EEO & Accommodations request here.
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