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 Clinical Research Supervisor (?CRS?) will be responsible for supervising the day-to-day activities of complex, possibly multi-site research projects focused on spine pathologies, spinal surgery techniques, and other spine-related interests.
The CRS will work closely with PIs and SCRC to ensure that clinical research studies are completed on time and within budget. They will also work with the research compliance officer to ensure that all staff and protocols are compliant with all guidelines.
Responsibilities
Leadership:
Responsible for the management and coordination of internal and external research projects
Ensures newly hired research coordinators are properly on-boarded and have completed the appropriate trainings
Mentor and provide best practices with more junior members of the research team
Oversees the coordination and creation of respective study protocols across the division
Responsible for the accuracy, thoroughness, quality, and timeliness of projects.
Supervise and participate in the integration, design, and development of new study protocols
Research Coordination:
Conducting clinical research protocols, including recruitment, enrollment and management of research subjects
Coordination of complex clinical trials
Research data collection, entry and database management
Assistance in research grant preparation and administration, including protocol development, consent form preparation, budgets and budget justifications, and submission of applications and progress reports
Assistance in regulatory reporting, compliance, and reporting of adverse events
Various administrative duties, financial transactions and reports
Assisting in the creation and implementation of monitoring systems for quality assurance
Arranging and coordinating the visit of the patient, including international patients
Other related responsibilities as necessary
Minimum Qualifications
Bachelor's degree or equivalent in education and experience, plus three years of related experience.
Preferred Qualifications
Prior research experience
Knowledge of Epic
Other Qualifications
Working knowledge of statistics and proficiency in Windows Operating environment and MS Word and Excel are required.
Willing to work some evenings and weekend hours.
Highly organized with great attention to detail.
Capable of prioritizing and managing several projects at once and taking responsibility for meeting deadlines.
Ability to lead and supervise several full-time and part-time students.
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
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.