Edtech.com's Summary

Columbia University is hiring a Data Coordinator to manage and reconcile data for clinical trials at the Herbert Irving Comprehensive Cancer Center's CPDM office. The role requires collaborating with clinical research teams to ensure data quality, integrity, and regulatory compliance while maintaining patient research records and coordinating monitoring activities.

Highlights

Manage and reconcile clinical trial data, ensuring completeness and accuracy.
Review research protocols and data at each study visit to resolve discrepancies.
Collaborate with research nurses, study coordinators, and Principal Investigators for data compliance.
Maintain patient research records and assist in gathering relevant clinical data.
Coordinate monitoring visits and document research meeting minutes.
Required qualifications: Bachelor's degree or equivalent education and experience.
Preferred experience in clinical research, knowledge of HIPAA and GCP guidelines.
Familiarity with paper Case Report Forms and electronic research databases.
Strong computer skills including proficiency in MS Word and familiarity with Mac and PC platforms.
Salary range: $64,350 - $67,000 annually.

Data Coordinator Full Description

Job Type: Officer of Administration
Bargaining Unit:
Regular/Temporary: Regular
End Date if Temporary:
Hours Per Week: 35
Standard Work Schedule:
Building:
Salary Range: $64,350 - $67,000

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.

Position Summary

The Data Coordinator manages and reconciles data for clinical trials conducted through the Herbert Irving Comprehensive Cancer Center, CPDM office. This position reports to directly to the Clinical Research Manager of the specific disease site this incumbent is assigned to.
This position is located at the Fort Lee, NJ office.

Responsibilities

DATA MANAGEMENT

Reviewing research protocols for appropriate data management.
Reviewing data at each study visit for completeness, the reconciliation of data queries and discrepancies, prospective data entry of ongoing research activities, and other activities related to data management.
Working with the research nurse, study coordinators, and Principal Investigators to ensure data quality, integrity and compliance with all regulatory institutional and department requirements.
Maintaining patient research records and will work in conjunction with a study team to gather all required data and relevant clinical information.
Working with the study team to resolve any outstanding items.

OTHER

Coordination of monitoring visits.
Documentation and maintenance of research meeting minutes.
Performs other related duties and participates in special projects as assigned.

Minimum Qualifications

Bachelor’s degree or equivalent in education and experience.

Preferred Qualifications

Experience in clinical research setting with knowledge of HIPAA and GCP.
Experience with paper Case Report Forms (CRFs) and/or electronic research databases.
Knowledge of medical terminology and procedures specifically related to oncology.
Strong critical thinking and problem-solving skills.
Ability to work independently in a fast-paced environment.
Ability to exercise professional judgment and discretion in dealing with confidential matters.
Computer Skills: proficiency with MS Word programs and familiarity with Mac and PC platforms.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

Original Job Description

Job Type: Officer of Administration
Bargaining Unit:
Regular/Temporary: Regular
End Date if Temporary:
Hours Per Week: 35
Standard Work Schedule:
Building:
Salary Range: $64,350 - $67,000

Position Summary

Responsibilities

DATA MANAGEMENT

Reviewing research protocols for appropriate data management.
Reviewing data at each study visit for completeness, the reconciliation of data queries and discrepancies, prospective data entry of ongoing research activities, and other activities related to data management.
Working with the research nurse, study coordinators, and Principal Investigators to ensure data quality, integrity and compliance with all regulatory institutional and department requirements.
Maintaining patient research records and will work in conjunction with a study team to gather all required data and relevant clinical information.
Working with the study team to resolve any outstanding items.

OTHER

Coordination of monitoring visits.
Documentation and maintenance of research meeting minutes.
Performs other related duties and participates in special projects as assigned.

Minimum Qualifications

Bachelor’s degree or equivalent in education and experience.

Preferred Qualifications

Experience in clinical research setting with knowledge of HIPAA and GCP.
Experience with paper Case Report Forms (CRFs) and/or electronic research databases.
Knowledge of medical terminology and procedures specifically related to oncology.
Strong critical thinking and problem-solving skills.
Ability to work independently in a fast-paced environment.
Ability to exercise professional judgment and discretion in dealing with confidential matters.
Computer Skills: proficiency with MS Word programs and familiarity with Mac and PC platforms.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

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