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Be ready to walk through monitoring visit types, CAPA examples, risk-based monitoring, and how you escalate safety or quality issues. Expect FSP-specific questions on working inside a sponsor model while employed by Parexel, plus travel readiness for a Texas/Central U.S. territory.
Strong fit if you have multi-site CRA experience, comfort with FSP/client structures, and willingness to cover a Central U.S. footprint. Thin public culture signal in the data—lean on your own network and the interview for team fit.
As a Senior Clinical Research Associate (FSP) at Parexel covering Texas/Central U.S., expect site monitoring, protocol and GCP compliance checks, source data verification, query resolution, and sponsor-facing status updates across assigned investigator sites—coordinating with Parexel clinical ops and the client study team rather than pure desk work in Providence.
Build monitoring, GCP, and therapeutic-area fluency. Free learning options:
Parexel is a CRO that designs and runs clinical trials for pharma and biotech clients.
The listing is not marked remote (remote = 0); expect field/site work for a Texas/Central U.S. FSP CRA, with the posted location in Providence, RI.
Saylor Academy Health Sciences courses are free; Coursera audit-track healthcare courses are free to learn.
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.
Public cache only — not an employee review.
Parexel is hiring a Senior Clinical Research Associate (FSP) based in Providence, Providence County, to drive site monitoring and management excellence across clinical studies spanning Texas and the Central US region. About the Role As a Senior Clinical Research Associate at Parexel, you will support and oversee monitoring and site management activities for client-sponsored studies within a Functional Service Provider (FSP) model. Working from Providence, Providence County, you will ensure every study is conducted in full alignment with ICH GCP standards, country and local regulatory requirements, and client standard operating procedures (SOPs). Key Responsibilities Lead site monitoring and site management activities for client-sponsored clinical trials. Conduct both on-site and remote site visits, ensuring all interactions are accurately captured and documented in the CTMS. Verify that all study activities comply with ICH GCP, applicable regulations, and client-specific SOPs. Build strong, collaborative relationships with investigative sites and internal study teams. Monitor data quality, patient safety, and protocol adherence throughout the study lifecycle. Qualifications Proven experience as a Clinical Research Associate, with senior-level monitoring expertise. Thorough working knowledge of ICH GCP guidelines and relevant regulatory frameworks. Hands-on familiarity with CTMS and clinical trial documentation practices. Excellent communication and organizational skills for managing multiple sites simultaneously. Willingness to travel for on-site monitoring across the Texas and Central US territory. About Parexel Parexel is a global leader in clinical research, partnering with biopharmaceutical companies to bring new therapies to patients. Through our FSP solutions, our Senior Clinical Research Associates work as an integrated extension of our clients' teams, delivering quality, compliance, and scientific rigor at every stage of the trial process. How to Apply Ready to advance your clinical research career as a Senior Clinical Research Associate with Parexel in Providence, Providence County? View the full listing and apply here.
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