Our Ability Jobs

Employer Name: Columbia University

Job Type: Officer of Administration Bargaining Unit: Regular/Temporary: Regular End Date if Temporary: Hours Per Week: 20 Standard Work Schedule: Building: Salary Range: $34.29 - $36.00 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 Clinical Research Coordinator will assist in studies pertaining to women?s mental health. The Clinical Research Coordinator will work closely with the Principal Investigator and members of the overall research team. The position involves helping to coordinate clinical trials, maintenance and organization of the study databases, recruitment, and screening subjects. Individual will conduct phone contacts (scheduling and confirming study appointments), assist with study visits: psychophysiology lab sessions, fetal neurobehavioral assessment, blood draws, videotaping, RedCap data entry, and other study visits. Responsibilities Specific duties include but are not limited to: Completion of GCP, HIPPA and applicable regulatory training. Complete certification requirements for assigned protocols. Screen designated schedules or patient lists for eligible subjects. Approach and verify eligibility subjects. Consent and enroll eligible subjects. Complete research study visits as delineated in assigned protocol and manual of operations set forth by sponsor and supervisor. Complete Telephone follow-up and telephone reminder calls for study participants, during these phone calls the person will need to administer study questionnaire as assigned. Coordinate the collection of all research data points as assigned, whether through research visits, chart abstraction or telephone. Scheduling of research visits. Pick-up, processing, transporting, and shipping of biological specimens as assigned and following instructions delineated in the protocol or manual of operations. Completion of study documents and files; some examples might include case report forms, worksheets, and medical record notes. Maintain confidentiality of documents and files such as HIPPA. Informing relevant clinical staff regarding subject protocol participation. Assist in other research related activities and projects as needed. Regular collaboration with the PI and other research staff. Perform other related duties and responsibilities as assigned/requested. Minimum Qualifications Requires a bachelor?s degree or equivalent in education and experience. Bilingual either English/Spanish OR English/French. Preferred Qualifications Experience in clinical research or other relevant settings. Excellent interpersonal, written/oral communication, and organizational skills are required. Proficiency in Microsoft Office. Complete proficiency in written and spoken English. Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.