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Parexel
Parexel
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Parexel is a global clinical research organization serving biopharmaceutical companies throughout the development of new medicines. Its work spans Phase I–IV clinical trials, portfolio and trial management, regulatory strategy, market access, and lifecycle planning. With more than 21,000 professionals, Parexel combines clinical, regulatory, and therapeutic expertise with patient insights and innovative trial designs. The company supports research across areas including oncology, neuroscience, and rare diseases, with a focus on making clinical development more efficient and patient-centered.
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Clinical Research Associate II / Senior Clinical Research Associate — Remote, Arizona

Oversee investigator sites and monitor clinical trials for Parexel, supporting patient safety, GCP compliance, recruitment, and study quality. The role covers sites across the United States and is listed as remote in Arizona.

USUnited StatesAZArizonaRemoteFull-timeJuniorMiddleEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Oversee investigator sites throughout clinical trials, from site management and monitoring to close-out.
  • Protect patient safety and maintain study quality in line with applicable laws, GCP, and sponsor standards.
  • Manage site relationships and operational work from site activation through database lock.
  • Act as the main contact for assigned sites and coordinate with Site Care Partners, study teams, vendors, and site staff.
  • Support site development, coaching, training, protocol education, and recruitment.
  • Monitor sites on-site and remotely or electronically during initiation, routine follow-up, and closure.
  • Track adverse events and serious adverse events, working with the Drug Safety Unit.
  • Submit TMF records, site reports, follow-up letters, protocol deviations, recruitment updates, clinical supply details, study progress, and metrics.
  • Identify and address site issues, and develop corrective and preventive actions.
  • Resolve data queries and complete investigator site close-out activities.
  • Oversee investigational product receipt, handling, accountability, storage, and destruction.
  • Support database release and, when appropriate, carry out unblinded monitoring duties.
  • Maintain knowledge of products, protocols, and therapy areas to support patient safety and clinical guidance.
  • Lead quality-event remediation and audit CAPA activities when applicable.

Requirements

  • Bring extensive knowledge of clinical trial methods, ICH/GCP, FDA rules, and local regulations.
  • Have at least two years of relevant experience monitoring clinical research sites.
  • Be fluent in English and the native language or languages of the country where you will work.
  • Be able to travel 60–80% of the time.
  • Hold a valid driver’s license and passport.
  • Have a bachelor’s degree in life sciences or an equivalent professional life sciences qualification, such as nursing, pharmacy, or a medical background.

Benefits

  • Equal opportunity consideration regardless of legally protected status.
  • The role requires substantial travel; no specific travel allowance or compensation is stated.

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