Oncology Clinical Research Coordinator — Growth & Certification

Ohio State University

Columbus (OH)

On-site

USD 52,000 - 76,000

Full time

14 days+
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Job summary

The Ohio State University’s James Cancer Hospital and Solove Research Institute seeks a Clinical Research Coordinator to support oncology trials. You will assist with patient records, consent, data collection, and study coordination across multiple OSU locations.

The role requires a bachelor’s degree in biological or related fields, strong communication, and experience in clinical research; SoCRA/ACRP certification is preferred.

Qualifications

  • Bachelor’s Degree in biological sciences or related field required.
  • One year of clinical research experience is required.
  • Knowledge of medical terminology desired.
  • Clinical research certification from SoCRA/ACRP is preferred.
  • Computer skills with Microsoft Office applications required.

Responsibilities

  • Assist with assessing patient records to identify eligibility for protocols.
  • Recruit, interview and enroll patients.
  • Obtain informed consent and ensure consent process compliance.
  • Educate patients and families about study purpose, goals, and processes.
  • Coordinate scheduling of patient visits, procedures and tests per protocol.
  • Monitor patients for adverse reactions and report to appropriate clinicians.
  • Document unfavorable responses and notify sponsors and regulatory agencies.
  • Assist with collecting, extracting, coding, and analyzing research data.
  • Support IRB and sponsor regulatory compliance and reviews.
  • Prepare for external quality assurance and audits.

Skills

Communication skills
MS Office
Medical terminology

Education

Bachelor’s Degree in biological sciences or related field

Job description

The Ohio State University’s James Cancer Hospital and Solove Research Institute seeks a Clinical Research Coordinator to support oncology trials. You will assist with patient records, consent, data collection, and study coordination across multiple OSU locations.

The role requires a bachelor’s degree in biological or related fields, strong communication, and experience in clinical research; SoCRA/ACRP certification is preferred.

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