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9d ago Curated

Clinical Research Associate

Pfizer
  • Other
  • Full-time
  • 2+ years

Job description

The Clinical Research Associate is responsible for site management, monitoring, and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable laws, Good Clinical Practices, and Pfizer standards. Duties include conducting onsite and remote monitoring, managing investigator site relationships, ensuring protocol compliance, monitoring adverse events, resolving data queries, and supporting database release. Requires a bachelor's degree in life sciences or professional degree such as nursing, pharmacy, or medical background. Significant travel (60-80%) within area is required; may include international travel. Valid driver's license and passport required.

Key responsibilities

  • Conduct site initiation, routine monitoring, and close-out visits (onsite and remote)
  • Serve as primary point of contact for assigned investigator sites
  • Monitor site-level AEs and SAEs, collaborate with Drug Safety Unit
  • Submit required reports and documentation within required timeframes
  • Resolve data queries and ensure investigator site compliance

What you bring

  • Knowledge of clinical trial methodologies, ICH/GCP, FDA regulations
  • Monitoring experience in clinical research
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases
  • Fluent in English

Tags

Field-BasedClinical ResearchSite MonitoringTravel Required

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