Clinical Research Coordinator II — Trials & Data Specialist

Columbia University Irving Medical Center; New York (NY); On-site; USD 69,000 - 71,000; Full time

Job summary

Columbia University Irving Medical Center in New York seeks a Clinical Research Assistant to support day-to-day research activities in the Department of Anesthesiology. The role reports to the PI and will manage recruitment, data entry, and study coordination for ALPACA and other studies.

This is a full-time, funded position with continuation depending on funding. Responsibilities include maintaining study files, communicating with subjects and sponsors, and ensuring compliance with safety and

Qualifications

• Bachelor’s degree or equivalent and relevant experience required.
• Strong analytical and communication skills.
• Ability to work with minimal supervision and in a deadline-driven environment.
• Experience coordinating clinical research activities.
• Proficiency in maintaining study documents and data entry.

Responsibilities

• Coordinate day-to-day study protocol tasks including recruitment and follow-up.
• Maintain clinical research files and data integrity.
• Communicate with study subjects, clinicians, sponsors and staff.
• Prepare data reports and ensure compliance with processes.
• Support training and certifications for the team.

Skills

Critical thinking

Analytical skills

Oral and written communication

Team coordination

Independent work

Time management

Education

Bachelor’s degree or equivalent

2-3 years equivalent in education, training and experience in a relevant clinical research field

Phlebotomy-certified or willingness to become certified

Previous clinical, patient-oriented research experience

Experience in acute-care environments

Experience with biological specimen collection and handling

Job description

Columbia University Irving Medical Center in New York seeks a Clinical Research Assistant to support day-to-day research activities in the Department of Anesthesiology. The role reports to the PI and will manage recruitment, data entry, and study coordination for ALPACA and other studies.

This is a full-time, funded position with continuation depending on funding. Responsibilities include maintaining study files, communicating with subjects and sponsors, and ensuring compliance with safety and