Senior Clinical Research Associate – Texas – FSP

Join Parexel as a Senior Clinical Research Associate in Carson City, where you'll lead critical clinical trial oversight and drive investigator site excellence. This full-time position offers the opportunity to shape patient safety and data integrity across complex, high-stakes research programs.

About the Role

As a Senior Clinical Research Associate, you'll manage the complete lifecycle of assigned investigator sites from protocol initiation through study close-out. Your work ensures that every site operates at the highest standards of Good Clinical Practices (GCP), maintains rigorous compliance with applicable regulations, and delivers the quality and precision our sponsors demand. You'll be the clinical research leader at your assigned sites, balancing site support with thorough, evidence-based monitoring to protect patient welfare and study integrity.

What You'll Do

• Conduct comprehensive site monitoring visits to verify protocol adherence, verify data accuracy, and assess patient safety protocols
• Lead site initiation activities, including investigator qualification, staff training, and regulatory documentation review
• Evaluate and report on adverse events, safety signals, and protocol deviations with precision and timeliness
• Build and maintain effective communication with site investigators, coordinators, and sponsor teams to resolve issues and keep studies on track
• Audit source documentation and study records to confirm completeness, accuracy, and regulatory compliance
• Coordinate study close-out procedures, including final reconciliation, regulatory archiving, and site closeout documentation
• Mentor and support site staff on protocol requirements, CRA expectations, and compliance best practices
• Document monitoring activities and escalate concerns through appropriate channels to ensure sponsor notification

What We're Looking For

• 3+ years of clinical research experience in a monitoring or quality assurance role
• Comprehensive knowledge of Good Clinical Practices, ICH guidelines, and FDA regulations
• Proven ability to manage multiple sites independently and prioritize competing demands
• Strong attention to detail and demonstrated ability to identify gaps in data integrity or protocol compliance
• Excellent interpersonal skills with the ability to train, support, and influence site teams
• Proficiency with clinical trial software and data management systems
• Bachelor's degree in life sciences, clinical research, or related field

About Parexel

Parexel is a leading clinical research organization committed to advancing public health through innovative trial designs and rigorous patient safety protocols. We support biopharmaceutical sponsors in bringing life-changing therapies from concept to patient.

How to Apply

To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.