Senior Professional Research Assistant
Job description
Description
University of Colorado – School of Medicine
Senior Professional Research Assistant
The University of Colorado Denver l Anschutz Medical Campus seeks individuals with demonstrated commitment to creating an inclusive learning and working environment. We value the ability to engage effectively with students, faculty and staff of diverse backgrounds.
The Department of Orthopedics, Spine Division has an opening for a full time Senior Professional Research Assistant (PRA ). The PRA will serve as the Research Coordinator/Regulatory Manager for clinical studies. This position will assist faculty with all aspects of administrative activities related to the submission of Institutional Review Board (IRB) protocols to the Colorado Multiple Institutional Review Board (COMIRB), Western IRB (WIRB), and other regulatory agencies. This includes protocol development, writing consent forms, adverse event reporting, and managing continuing reviews of protocols. The PRA will ensure compliance with all internal and external policies and procedures that govern the department's human subject’s research. This includes monitoring FDA-IDE trials. The PRA will interact with patients during study visits and ensure completion of all necessary documentation, as well as facilitating study-related billing. The PRA will serve as a liaison to study sponsors and will lead site visits. The PRA will also assist in the development and maintenance of a record keeping system of protocols for COMIRB and other regulatory agency activities.Primary Duties and Responsibilities include:- Oversee clinical trials research, including all sponsored studies
- Oversee on-going research projects on a daily basis
- Oversee the other research staff including PRAs, research assistant, and employed/volunteer students
- Maintain and oversee the completion of records of all research projects
- Track upcoming patient study visits
- Assist in design and submission of future research protocols
- Interact with institutional review board for protocols
- Interact with sponsors regarding clinical studies
- Interact with patients during study visits
- Maintain database of clinical studies
- Assist with preparation of manuscripts and research presentations
- Assist with preparation of grants and project reports
- Provide additional support to the Principal Investigators as needed
- Oversee and assist trainees (fellows, residents, and students) with development and continuation of research projects
Qualifications
Knowledge, Skills and Abilities
- Good command of the English language, both written and verbal
- Excellent computer skills
- Excellent knowledge regarding IRB policies and procedures
- Excellent knowledge regarding Sponsor and FDA regulatory requirements
- Excellent communication skills, both written and verbal
- Ability to problem solve and multi-task.
- Ability to work with a great attention to detail
- Ability to work with colleagues and patients in a confidential and professional manner
- Master's degree in healthcare administration, research services or a related field
- Minimum of 7 years’ experience with clinical research
Job Category: Faculty
Primary Location: Aurora
Schedule: Full-time
Posting Date: Apr 2, 2021
Unposting Date: Ongoing