Senior Clinical Research Associate
Core
Managing investigator sites throughout the clinical trial lifecycle to ensure patient safety, quality study execution, and regulatory compliance.
Role type
Senior Clinical Research Associate (Site Monitoring)
Builds
Clinical trials for pharmaceutical products
Domain
Healthcare / Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical trial site monitoring, GCP/ICH/FDA regulations, Adverse event management, Protocol deviation handling, Site activation and enrollment support, Investigational product oversight, Audit readiness, Corrective and preventive action planning
Preferred skills
Oncology, Vaccines, Internal Medicine, or Infectious Diseases therapeutic experience, Global clinical trial experience
Technologies
Electronic monitoring systems
Responsibilities
Conduct on-site, remote, and electronic monitoring visits (initiation, routine, closeout); Review and follow up on adverse events (AEs) and serious adverse events (SAEs); Resolve data queries and support database release; Mentor and train Clinical Research Associates; Participate in feasibility assessments and site selection activities. (via careerplan.io/jobs/4963166-1-senior-clinical-research-associate-at-pfizer)
Seniority
Senior, hands-on IC