Clinical Research Coordinator II - Oncology

Schuylkill•Allentown, PA
•Onsite

About The Position

Plans, initiates, coordinates, implements, and oversees clinical trials in the Oncology division of the Network Office of Research and Innovation. Coordinates care for research patients with multiple disease processes in collaboration with healthcare professionals, ensuring timely, high-quality care across the care continuum.

Requirements

  • Bachelor’s degree in science, nursing, or health care.
  • Ability to initiate, accept, and adapt to change.
  • Pennsylvania Registered Nurse license required upon hire.

Nice To Haves

  • Two years of research experience.
  • Two years of direct clinical experience in an acute care or healthcare setting.
  • Ability to mentor other research staff in clinical-trial conduct and regulatory compliance.
  • Oncology Certified Nurse (OCN) certification through ONCC.
  • Certified Clinical Research Coordinator (CCRC) certification through ACRP.
  • Certified Clinical Research Professional (CCRP) certification through SCRA.

Responsibilities

  • Plan, implement, and conduct approved clinical research trials.
  • Coordinate and manage patient assessments, phlebotomy, drug administration, and side-effect monitoring according to protocol standards and in a clinically safe, regulatory-compliant manner.
  • Assist in maintaining drug and medical device accountability according to regulatory guidelines.
  • Collect, record, and report data for assigned research studies.
  • Monitor sponsor and other agency visits to evaluate the accuracy and quality of collected data.
  • Attend all site initiation visits to become familiar with projects for cross-coverage purposes and support research initiatives.
  • Serve as a back-up coordinator for designated clinical trials.
  • Assist with NORI/IRB submissions and maintain regulatory, legal, and other required clinical-trial documentation.
  • Establish and maintain productive relationships with patients, family members, sponsors, and external contacts to optimize research outcomes.
  • Contribute to the healthcare team's development of the patient's plan of care.
  • Educate participants and staff about disease processes, therapies, and treatments being studied.
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