Clinical Research Coordinator I

Lehigh Valley Health Network•Allentown, PA
•Onsite

About The Position

Plans, initiates, coordinates, and implements minimal-risk studies in collaboration with other staff. Coordinates regulatory management of assigned clinical trials, processes and ships phlebotomy laboratory samples according to trial requirements, and collects, records, and reports research data. The role is based onsite at 1240 S Cedar Crest Blvd in Allentown and follows a Monday–Friday, 8:00 a.m.–4:30 p.m. schedule.

Requirements

  • Bachelor’s degree or five years of research experience.
  • Two years of experience in a clinical environment.
  • Self-motivated and organized, with the ability to ensure timely implementation of research protocols and successful outcomes.

Nice To Haves

  • Knowledge of medical terminology.
  • Knowledge of clinical research terminology.
  • Knowledge and skill in a therapeutic area and research.
  • CCRP-Cert Clinical Research Professional SCRA — State of Pennsylvania upon hire.
  • MLT — Medical Laboratory Technician AMT — State of Pennsylvania upon hire.

Responsibilities

  • Plan, implement, and conduct approved research studies and conduct and document informed consent for minimal-risk studies.
  • Perform phlebotomy and process, store, and ship laboratory samples as required by clinical research trials.
  • Coordinate regulatory management of assigned clinical trials, including assisting with NORI/IRB submissions, maintenance, and regulatory and legal documents.
  • Coordinate and manage patient assessments according to protocol standards.
  • Collect, record, and report data for research studies as assigned.
  • Maintain clinical research study documentation in collaboration with the Principal Investigator and study team.
  • Participate in sponsor and agency monitor visits to evaluate the accuracy and quality of collected data.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service