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

About the Program

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.

Position Summary

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.

Responsibilities

• 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.

Minimum Qualifications

• 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.

Preferred Qualifications

• 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).

Other Requirements

• 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.

About Columbia University

Columbia University is one of the world's most important centers of research and at the same time a distinctive and distinguished learning environment for undergraduates and graduate students in many scholarly and professional fields. The University recognizes the importance of its location in New York City and seeks to link its research and teaching to the vast resources of a great metropolis. It seeks to attract a diverse and international faculty and student body, to support research and teaching on global issues, and to create academic relationships with many countries and regions. It expects all areas of the university to advance knowledge and learning at the highest level and to convey the products of its efforts to the world.

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