Edtech.com's Summary

Columbia University is hiring a Project Coordinator to manage Alzheimer’s Disease and Related Disorders clinical trials and serve as the Alzheimer’s Clinical Trials Consortium Site Liaison. The role involves coordinating clinical trial activities, maintaining regulatory documentation, ensuring compliance with guidelines, and communicating with consortium and sponsor staff.

Highlights

Coordinate and conduct ADRD clinical trials under the principal investigator's direction.
Complete regulatory documentation and manage IRB submissions.
Consent participants, perform study procedures like ECGs, vital signs, blood draws, neuropsychological testing, and maintain source documents.
Serve as the primary liaison for ACTC projects, attending investigator and steering committee meetings.
Maintain compliance with GCP and FDA guidelines.
Manage participant recruitment, scheduling, reimbursement, and investigational product accountability.
Required certifications include CDR, Alzheimer’s Disease Assessment Scale, CANTAB, GDS, MoCA, NPI-Q, ADCS-ADL, and MMSE.
Bachelor’s degree or equivalent in education and experience required.
Preferred qualifications include 3 years of ADRD research experience, additional specialized certifications, and Spanish fluency.
Salary range: $64,350 - $68,000 annually.

Project 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: $64,350.00 - $68,000.00 annually

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

Study Coordinator for Alzheimer’s Disease and Related Disorders (ADRD) clinical trials.
Alzheimer’s Clinical Trials Consortium (ACTC) Site Liaison.

Responsibilities

Study Coordinator: Perform all study related procedures including but not limited to:

Conduct and coordinate consortium (ACTC/ADCS) and industry clinical trials in neurodegenerative disease under the direction of the principal investigator
Complete and maintain regulatory documentation
Initiate and maintain submissions for CUIMC IRB and central IRBs
Create and maintain source documents
Consent study participants according to CGP guidelines
Ensure that GCP and FDA guidelines are followed
Complete study-related data entry and chartings in a timely manner
Prepare study related correspondence
Perform study-related ECGs, vital signs and blood draws as necessary
Arrange research -related imaging and other auxiliary research related studies
Travel to investigator meetings as needed.
Ensure participant compliance to study protocol
Dispense and account for investigational product and research study samples
Arrange study participant reimbursement via the standard CU policies and procedures
Work with sponsor and consortium entities to ensure that all required duties are completed
Maintain productive working relationship between sponsor/consortium staff, study monitor, site staff and principal investigator
Perform neuropsychological and other testing scales and assessments
Recruit research participants by phone
Explain studies to potential participants by phone and in person
schedule appointments for research participants screening visits and regular study visit

ACTC Site Liaison:

Travel to investigator meetings
Primary point person across all the ACTC projects
Clinical trials coordinator for the ACTC projects
Attend ACTC Steering Committee Meetings three times a year
Participate in monthly ACTC Site Liaison Meetings

Minimum Qualifications

Bachelor's degree or equivalent in education and experience.
Certifications in CDR, Alzheimer’s Disease Assessment Scale Certification, CANTAB, GDS, MoCA, NPI-Q, ADCS-ADL, MMSE.

Preferred Qualifications

>3 years hands-on experience in ADRD research testing.
Certifications in CDR, C-SSRS, Alzheimer’s Disease Assessment Scale Certification, RBANS/, CTT, LNS, PF, GDS, MoCA, NTB, CIBIC-Plus and VaDAS, CANTABelect, CGIC, S-STS,CFT, Cogstate battery, NPI, ADCS-ADL, NPI, MMSE, TUG, CFT, LFT, CFT, NACC battery.
Spanish fluency.

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: $64,350.00 - $68,000.00 annually

Position Summary

Study Coordinator for Alzheimer’s Disease and Related Disorders (ADRD) clinical trials.
Alzheimer’s Clinical Trials Consortium (ACTC) Site Liaison.

Responsibilities

Study Coordinator: Perform all study related procedures including but not limited to:

Conduct and coordinate consortium (ACTC/ADCS) and industry clinical trials in neurodegenerative disease under the direction of the principal investigator
Complete and maintain regulatory documentation
Initiate and maintain submissions for CUIMC IRB and central IRBs
Create and maintain source documents
Consent study participants according to CGP guidelines
Ensure that GCP and FDA guidelines are followed
Complete study-related data entry and chartings in a timely manner
Prepare study related correspondence
Perform study-related ECGs, vital signs and blood draws as necessary
Arrange research -related imaging and other auxiliary research related studies
Travel to investigator meetings as needed.
Ensure participant compliance to study protocol
Dispense and account for investigational product and research study samples
Arrange study participant reimbursement via the standard CU policies and procedures
Work with sponsor and consortium entities to ensure that all required duties are completed
Maintain productive working relationship between sponsor/consortium staff, study monitor, site staff and principal investigator
Perform neuropsychological and other testing scales and assessments
Recruit research participants by phone
Explain studies to potential participants by phone and in person
schedule appointments for research participants screening visits and regular study visit

ACTC Site Liaison:

Travel to investigator meetings
Primary point person across all the ACTC projects
Clinical trials coordinator for the ACTC projects
Attend ACTC Steering Committee Meetings three times a year
Participate in monthly ACTC Site Liaison Meetings

Minimum Qualifications

Bachelor's degree or equivalent in education and experience.
Certifications in CDR, Alzheimer’s Disease Assessment Scale Certification, CANTAB, GDS, MoCA, NPI-Q, ADCS-ADL, MMSE.

Preferred Qualifications

>3 years hands-on experience in ADRD research testing.
Certifications in CDR, C-SSRS, Alzheimer’s Disease Assessment Scale Certification, RBANS/, CTT, LNS, PF, GDS, MoCA, NTB, CIBIC-Plus and VaDAS, CANTABelect, CGIC, S-STS,CFT, Cogstate battery, NPI, ADCS-ADL, NPI, MMSE, TUG, CFT, LFT, CFT, NACC battery.
Spanish fluency.

Equal Opportunity Employer / Disability / Veteran

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

Let me find your next job.

Thanks - you're signed up.

Project Coordinator

Edtech.com's Summary

Project Coordinator Full Description

ASSOCIATE DIRECTOR, Academic Support Svcs

Project Manager – Research Design & Development (Hybrid)

Director of Pre-K

Senior Program Administrator Supervisor

Executive Director