• Job Type: Officer of Administration
• Regular/Temporary: Regular
• Hours Per Week: 35
• Salary Range: $64,350 - $65,000

Position Summary

The Clinical Research Coordinator will support various research studies, encompassing government, private, and pharmaceutical initiatives. This position involves coordinating and executing clinical trials and protocols involving human subjects.

Responsibilities

• Study Subject Management: Streamline the screening, enrollment, and treatment processes for research subjects, ensuring compliance with established regulations, guidelines, and internal standard operating procedures.
• Assist with eligibility assessment and obtaining written informed consent as appropriate.
• Act as a liaison with sponsoring agencies and external sites.
• Facilitate sample collection, processing, and storage activities.
• Assist with regulatory submissions, including protocol review and monitoring.
• Assist with Research Billing Review (RBR) for research projects.
• Ensure that regulatory documents and administrative files for each protocol are up-to-date and adhere to sponsor requirements.
• Maintain Study Manager data entry for all assigned studies.
• Contribute to short-term projects and provide cross-coverage to various research team members as needed.
• Perform related duties and responsibilities as assigned or requested.

Minimum Qualifications

• Bachelor’s Degree or equivalent in education and experience
• Excellent organizational, writing, and verbal communication skills.

Preferred Qualifications

• At least two years relevant experience

Other Requirements

• 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.