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Posted: July 10, 2024
Salary:US$65000.00 - US$75000.00 per year
Location:Wyomissing Hills
Job type: Permanent
Discipline:Clinical Research
Work Location:On-site

Job description

Job Summary:

We are seeking a proactive and driven Clinical Research Coordinator (CRC) to join our dynamic clinical research team. The ideal candidate will have hands-on experience managing studies from start-up to close-out and a background in working within private clinical research settings. If you are a go-getter with a passion for clinical research and a proven track record in coordinating studies, we want to hear from you!

Key Responsibilities:

  • Coordinate and oversee all aspects of clinical trials from initiation to close-out, ensuring adherence to study protocols and regulatory requirements.
  • Proactively manage study timelines, deliverables, and resources to ensure successful study completion.
  • Recruit, screen, and enroll study participants according to inclusion and exclusion criteria.
  • Obtain informed consent from study participants and provide detailed information about study procedures.
  • Schedule and conduct study visits, collect data, and maintain accurate source documentation.
  • Perform study-related procedures, including vital signs, ECGs, blood draws, and other clinical evaluations as required by the protocol.
  • Monitor patient safety, report adverse events, and ensure timely follow-up with study participants.
  • Enter and manage study data in electronic data capture (EDC) systems, ensuring data integrity and accuracy.
  • Prepare for and participate in site monitoring visits, audits, and regulatory inspections.
  • Collaborate with investigators, study sponsors, and other research staff to ensure smooth study operations.
  • Maintain up-to-date knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
  • Provide exceptional patient care and maintain a positive, professional relationship with study participants.