• Job Type: Officer of Administration
• Bargaining Unit:
• Regular/Temporary: Regular
• End Date if Temporary:
• Hours Per Week: 35
• Standard Work Schedule:
• Building:
• Salary Range: 62,400.00 $68,000.00
  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.
  Position Summary
  The candidate must be highly motivated, be interested in pediatric neurological diseases, possess excellent interpersonal, communication, and writing skills as well as strong interest in academic clinical research. The candidate will be expected to establish cordial and professional rapport with children, adults and families as well as the clinical, research, and administrative teams. The ideal candidate is a team player who is also independently motivated and able to self-direct to complete tasks.
  The candidate will report to the Principal Investigator (PI), Dr. Jennifer Bain, and the clinical research supervisor. The candidate will be responsible for subject recruitment and proper conduct of clinical studies. Additional responsibilities include maintaining compliance with existing policies and procedures at Columbia University Irving Medical Center and its Institutional Review Board (IRB) and Clinical and Translational Science Center (CTSC), that regulate and conduct clinical research.

Responsibilities

• Participation in pre-study, initiation, monitoring and close-out visits
• Submission of Investigator New Drug (IND) forms and PI initiated research protocols to FDA and other regulatory institutions in US
• Implementation of clinical trials from initiation, including participation in the development of standard operating procedures and case report forms
• Recruitment and supervision of clinical trial subjects through the following activities: informed consent, screening, and ensuring subjects adherence to safety and study compliance issues.
• Coordination and management of clinical trials, communication with sponsor and monitors, study visit coordination, sample acquisition and processing.
• Reporting and documentation of protocol deviations and exemptions as well as development and implementation of corrective action plans for review by the Principal Investigator as needed
• Data collection and management, collection of source documents, registration, and management of adverse events, filing and archiving, managing monitoring visits and managing queries.
• Participate in data entry and query resolution using Electronic Data Capture (EDC) systems
• Close-out of the clinical trial, contributing to manuscripts, audit preparation, trial completion, and communication with authorities. Other responsibilities include assisting with the final study report and completing financial obligations.
• Other duties assigned as needed by the division.

Minimum Qualifications

• Requires a bachelor’s degree or equivalent in education and experience.

Preferred Qualifications

• 1 Year of research experience. Undergraduate experience is acceptable.

Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents

• Participation in pre-study, initiation, monitoring and close-out visits
• Submission of Investigator New Drug (IND) forms and PI initiated research protocols to FDA and other regulatory institutions in US
• Implementation of clinical trials from initiation, including participation in the development of standard operating procedures and case report forms
• Recruitment and supervision of clinical trial subjects through the following activities: informed consent, screening, and ensuring subjects adherence to safety and study compliance issues.
• Coordination and management of clinical trials, communication with sponsor and monitors, study visit coordination, sample acquisition and processing.
• Reporting and documentation of protocol deviations and exemptions as well as development and implementation of corrective action plans for review by the Principal Investigator as needed
• Data collection and management, collection of source documents, registration, and management of adverse events, filing and archiving, managing monitoring visits and managing queries.
• Participate in data entry and query resolution using Electronic Data Capture (EDC) systems
• Close-out of the clinical trial, contributing to manuscripts, audit preparation, trial completion, and communication with authorities. Other responsibilities include assisting with the final study report and completing financial obligations.
• Other duties assigned as needed by the division