Clinical Research Coordinator - Hematology & Oncology

Clinical Research Coordinator - Hematology & Oncology

Join to apply for the Clinical Research Coordinator - Hematology & Oncology role at Columbia University Irving Medical Center

Grade: 103
Job Type: Officer of Administration
Regular/Temporary:
Regular
Hours Per Week: 35
Salary Range: $66,300 - $75,000

The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.

The Columbia Amyloidosis Multidisciplinary Program (CAMP) is a collaborative clinical and research initiative that brings together experts in hematology, nephrology, cardiology, and neurology to advance the understanding, diagnosis, and treatment of amyloidosis. CAMP integrates patient care with translational and clinical research to improve outcomes and develop innovative therapeutic approaches for individuals affected by this complex disease.

The Columbia Amyloidosis Multidisciplinary Program (CAMP) is seeking a Clinical Research Coordinator (CRC) to support its expanding clinical and translational research portfolio. The CRC will coordinate day-to-day research operations, including patient recruitment, data collection, and regulatory compliance, while working closely with investigators and clinical teams across multiple disciplines. This position offers the opportunity to contribute to innovative research aimed at improving the diagnosis and treatment of amyloidosis.

The CRC will report to the Director of the Multiple Myeloma and Amyloidosis Program and work closely with investigators, clinical staff, and external collaborators.

• Work Schedule:
  
  Monday–Friday, full-time.
• Work Location:
  
  Onsite at Columbia University Irving Medical Center.

• Coordinate and implement research protocols in collaboration with investigators and clinical staff.
• Recruit, screen, and consent study participants in accordance with IRB-approved protocols.
• Collect, process, and manage clinical data and biospecimens; administer study questionnaires.
• Maintain accurate and timely documentation in electronic data capture systems and case report forms.
• Ensure compliance with institutional, federal, and sponsor regulations (e.g., IRB, GCP, HIPAA).
• Monitor data quality and resolve discrepancies in collaboration with data coordinating centers.
• Assist with IRB submissions, amendments, and continuing reviews.
• Communicate effectively with internal and external stakeholders to support study progress.
• Perform additional related duties as assigned.

• Bachelor’s degree or equivalent combination of education and experience.
• Strong organizational, communication, and interpersonal skills.
• Ability to work independently and collaboratively in a multidisciplinary environment.
• High attention to detail and commitment to data integrity and regulatory compliance.

• Prior experience in clinical research, patient coordination, or data management.
• Familiarity with IRB processes, Good Clinical Practice (GCP), and electronic data capture systems (e.g., REDCap, Medidata).

• Medical clearance and participation in the medical surveillance program.
• Contact with patients and/or human research subjects.
• Successful completion of applicable compliance and systems training requirements.

Equal Opportunity Employer / Disability / Veteran:
Columbia University is committed to the hiring of qualified local residents.