Clinical Research Coordinator I: Start in Dynamic Trials

Lehigh Valley Health Network, Inc.

Allentown (Lehigh County)

On-site

USD 60,000 - 75,000

Full time

4 days ago
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Job summary

Lehigh Valley Health Network in Allentown, PA seeks a Clinical Research Coordinator I to join the NORI team and manage minimal risk studies and regulatory tasks.

You will coordinate informed consent, phlebotomy for trial samples, and data collection in collaboration with the study team, under the PI's guidance. A Bachelor’s degree or 5 years of research experience is required, with relevant certifications preferred.

Qualifications

  • Bachelor’s Degree or 5 years of research experience.
  • 2 years of experience in a clinical environment.
  • Must be self-motivated and organized to ensure timely implementation of research protocols and successful outcomes.

Responsibilities

  • Plan, initiate, coordinate, and conduct approved research studies and conduct and document informed consent process for minimal risk studies.
  • Performs phlebotomy and processes, stores, and ships laboratory samples as required by the Clinical Research Trials.
  • Coordinates the regulatory management of assigned clinical trials by assisting with NORI/IRB submissions, maintenance, and regulatory and legal documents.
  • Coordinates and manages the patient assessments according to protocol standards.
  • Collects, records, and reports data for research studies, as assigned.
  • Maintains documentation for clinical research studies, working with the Principal Investigator and study team, and participates in monitor visits with sponsors and other related agencies to evaluate the accuracy and quality of the collected data.

Skills

Self-motivated
Organized

Education

Bachelor’s Degree

Tools

CCR P Certification
SCRA Certification
AMT Certification

Job description

Lehigh Valley Health Network in Allentown, PA seeks a Clinical Research Coordinator I to join the NORI team and manage minimal risk studies and regulatory tasks.

You will coordinate informed consent, phlebotomy for trial samples, and data collection in collaboration with the study team, under the PI's guidance. A Bachelor’s degree or 5 years of research experience is required, with relevant certifications preferred.

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