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Clinical Research Associate / Senior Clinical Research Associate - FSP

Parexel · Washington, D.C., US

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Company facts (cached)

Website: parexel.com

Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress.

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Role overview (listing rewrite)

Parexel is hiring a full-time Clinical Research Associate or Senior Clinical Research Associate to lead clinical trial operations at research sites in Washington, D.C. If you have oncology expertise and interest in cell therapy research, this on-site role offers the opportunity to drive protocol compliance and participant safety in a collaborative, fast-paced environment. About the Role In this Clinical Research Associate position, you'll own primary responsibility for study execution at assigned research sites. You'll serve as the key liaison between the trial sponsor, site staff, and Parexel's central team—ensuring every aspect of the trial runs smoothly, data remains accurate, and all regulatory standards are met. What You'll Do Oversee day-to-day study operations at designated sites, managing protocol timelines, documentation, and regulatory compliance Collaborate with site investigators, coordinators, and peer Clinical Research Associates to deliver high-quality trial data and maintain rigorous standards Conduct regular site visits to monitor protocol adherence, verify source documentation, and resolve compliance gaps Support participant recruitment and enrollment, ensuring informed consent and ongoing safety monitoring Maintain comprehensive study records and produce progress reports on site performance and trial milestones Communicate transparently with the study team, escalating issues and implementing solutions in real time What We're Looking For Demonstrated experience as a Clinical Research Associate in oncology trials (required) Hands-on background in cell therapy research (strongly preferred) Solid grasp of Good Clinical Practice (GCP) standards and FDA regulatory requirements Strong organizational and interpersonal skills with the ability to juggle multiple priorities Self-directed work style balanced with proven ability to thrive in collaborative team settings Commitment to detail and data integrity in every aspect of trial execution About Parexel Parexel is a global clinical research organization dedicated to advancing innovative therapies and improving patient outcomes. Our Field Safety Program brings specialized expertise in site management and trial oversight across therapeutic areas including oncology and emerging cellular therapies. How to Apply Interested in joining Parexel in Washington, D.C.? Submit your application through this listing today.

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