"Senior Research Coordinator"

Position Summary

The position is responsible for collaborating with Principal Investigators (PI) and their team as well as working independently to coordinate clinical research studies and trails. The research team is highly synergistic and works in a fast-paced, dynamic environment to advance knowledge in pediatric heart disease. This role is well-suited for an energetic self-starter who enjoys learning and the challenge of solving problems that improve people’s lives. The candidate would report to the PI and the Director of Research for the Clinical Research Core in the Department of Pediatrics. The senior research coordinator will have strong organizational, multi-tasking, time management, communication, and team skills to join our team in the assessment of outcomes, value of care, and health inequities for children for congenital heart disease.

At CUIMC, we are leaders in teaching, research, and patient care and are proud of the service and support we provide to our community. Columbia University offers a range of benefits to help you, and your dependents stay healthy, build long-term financial security, meet educational and professional goals, and more. Explore your options for Health and Welfare, Employee Assistance, Tuition Programs, and Retirement Benefits.

"Subject to business needs, we may support flexible and hybrid work arrangements. Options will be discussed during the interview process".

Responsibilities

• Working directly with the PIs and other team members to prioritize day-to-day study operations and direct investigations.
• Identifying and screening potential participants to determine eligibility.
• Participate in the informed consent process, randomizing participants and completing case report forms.
• Assisting with scheduling of tests and appointments.
• Managing data collection and submission and maintaining relevant databases; consulting medical records as necessary to obtain pertinent data.
• Collecting, processing, and shipping protocol specimens.
• Preparing/monitoring study budgets and regulatory documents for IRB submissions, data use agreements, and contracting.
• Directing communications with patients and collaborators.
• Assisting with grant and manuscript writing.
• Develop plans for protocol implementation, identify necessary resources and request as appropriate. This includes instruments, equipment and staff.
• Assist the Research Manager in the preparation of study budgets, research related cost estimate forms, and initiation of all new adult research studies and trials.
• Provide assistance to all other research staff members that are involved in the research trials and studies.
• Performs related duties & responsibilities as assigned/requested.

Minimum Qualifications

• Bachelor’s degree or equivalent in education and experience required; plus three years of related experience.

Preferred Qualifications

• Excellent verbal and written communication and interpersonal skills.
• Strong organizational and time management skills.
• Proficiency in MS Office, specifically Word, Excel, PowerPoint, and Outlook, is required.
• Familiarity with reviewing electronic medical records.
• Previous or active CCRC/CCRP certification is preferred.

Salary Range

$67,000.00 - $75,000.00

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.

Other Details

• Job Type: Officer of Administration
• Regular/Temporary: Regular
• Hours Per Week: 35