Clinical Research Coordinator | Columbia University Job at Columbia University, New York, NY

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  • Columbia University
  • New York, NY

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 - $68,650

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

We are looking for someone who can establish good rapport with children, adults and families as well as the clinical, research, and administrative teams. We emphasize the importance of team unity as central to our success.

The candidate will report to the Principal Investigator (PI) and the research supervisor and will be responsible for subject recruitment and the conduct of clinical studies. Additional responsibilities include maintaining compliance with existing policies and procedures at Columbia University, the IRB, and the CTSA, that relate to clinical research.

Responsibilities

  • Participation in pre-study, initiation, monitoring and close out visits
  • Submission of FDA IND studies and PI initiated research protocols to other regulatory institutions in US 
  • Implementation of clinical trials from initiation, including assistance with the development of standard operating procedures and case report forms
  • Recruitment and coordination of the clinical trial participants covering informed consent, screening, and inclusion of the subjects adhering to safety and compliance issues.
  • Coordination and management of the clinical trial, communication with sponsor and monitors, 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.
  • Close-out of the clinical trial, contributing to manuscripts, audit preparation, trial completion, and communication with authorities.
  • Additional 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.

Other Requirements

  • The candidate should be highly motivated, interested in pediatric neurological diseases, have excellent interpersonal skills and an interest in academic research.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residen ts.

About Columbia University

Columbia University is one of the world's most important centers of research and at the same time a distinctive and distinguished learning environment for undergraduates and graduate students in many scholarly and professional fields. The University recognizes the importance of its location in New York City and seeks to link its research and teaching to the vast resources of a great metropolis. It seeks to attract a diverse and international faculty and student body, to support research and teaching on global issues, and to create academic relationships with many countries and regions. It expects all areas of the university to advance knowledge and learning at the highest level and to convey the products of its efforts to the world.

Connections working at Columbia University

Job Tags

Temporary work, Local area,

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