Clinical Research Coordinator I

Columbia University Irving Medical Center is hiring a Clinical Research Coordinator I to provide research, regulatory, and administrative support for studies on medical device accessibility and the preferences of individuals with disabilities. The role coordinates participant recruitment and study activities, data collection and management, regulatory compliance, and research operations.

Responsibilities

Coordinate and support research activities in accordance with study protocols, institutional policies, and regulatory requirements

Maintain compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB), and sponsor requirements

Assist with the preparation, submission, and maintenance of IRB applications, continuing reviews, amendments, and study reports

Support the development and implementation of surveys, discrete choice experiments, and other study instruments

Assist with testing and maintaining web-based research tools and accessible survey platforms

Conduct literature reviews and market research to support study activities and medical device selection

Assist with the implementation and evaluation of the MED-AUDIT accessibility assessment software

Develop study materials, training resources, and participant-facing communications as needed

Recruit, screen, and enroll research participants according to study eligibility criteria and protocol requirements

Maintain ongoing communication with study participants and coordinate study visits, follow-up activities, and data collection

Track participant enrollment, retention, and compensation

Collect, enter, verify, and maintain study data using electronic databases and research management systems

Organize and maintain study records, regulatory documentation, and research databases

Coordinate activities of student assistants and other research support personnel as assigned

Assist with data summaries, presentations, reports, manuscripts, and other dissemination activities

Manage study supplies, equipment, and research-related materials

Assist with purchasing, inventory management, and other administrative functions supporting research operations

Perform additional related duties and responsibilities as assigned

Preferred

Master's degree

doctoral degree (PhD or equivalent)

Experience conducting human subjects research and managing IRB-regulated studies

Experience with laboratory or research supply procurement and inventory management

Familiarity with laboratory safety procedures, biosafety practices, and compliance documentation

Experience supervising, mentoring, or training student researchers or research staff

Demonstrated ability to work independently while managing multiple projects and competing deadlines

Master’s Degree

Doctoral Degree

IRB-Regulated Studies

Research Procurement

Inventory Management

Laboratory Safety

Biosafety Practices

Compliance Documentation

Research Staff Supervision

Researcher Training

Multitasking

Deadline Management

Mentoring

Company

Academic medical center providing patient care, research, and education.

New York, New York, USA

https://www.cuimc.columbia.edu/

Founded in 1767

10001+ employees

Qualifications

Bachelor's degree or an equivalent combination of education, training, and experience

Experience working with individuals with disabilities and knowledge of accessibility principles and practices

Experience leading or coordinating software, application, or technology development projects

Proficiency in Python, R, SAS, or similar programming languages for research design, data processing, and analysis

Strong organizational, communication, and project management skills

Ability to work independently and collaboratively within a team environment

Strong analytical and problem-solving skills

Excellent interpersonal, verbal, and written communication skills

Knowledge of clinical and human subjects research regulations and procedures

Attention to detail and commitment to data quality and accurate recordkeeping

Ability to maintain professionalism, confidentiality, and respect for participants' rights, privacy, and individual needs

Experience managing research databases and electronic data systems

Master's degree

Doctoral degree (PhD or equivalent)

Experience conducting human subjects research and managing IRB-regulated studies

Experience with laboratory or research supply procurement and inventory management

Familiarity with laboratory safety procedures, biosafety practices, and compliance documentation

Experience supervising, mentoring, or training student researchers or research staff

Demonstrated ability to work independently while managing multiple projects and competing deadlines

Required skills

Represents the skills you have, click on the tags, Accessibility Principles, Software Development Project Coordination, Python, R, SAS, Human Subjects Research, IRB-Regulated Studies, Biosafety

Preferred skills

Master's degree, doctoral degree (PhD or equivalent), Glassdoor, 3.5, New York, New York, USA, https://www.cuimc.columbia.edu, Late Stage, Leadership Team, Donna Lynne, Senior Vice President and COO, Recent News, Genetic Engineering News, 2026-05-30, News-Medical.Net, 2026-05-29, PR Newswire, 2026-04-23, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

Entry level