Research Services Principal Pr
About The Position
The School of Medicine Department of Orthopedics has an opening for a Research Services Principal Professional. Principal Clinical Science Professionals perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Principal Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. Principal Clinical Science Professionals either act as work/team leads for 2 or more FTE Professionals, operate as Clinical Research Nurses (RN), or are the subject matter experts (SME) in a particular area. SMEs possess a deep knowledge and oversight of a specific process, function and/or technology. SMEs are considered an authority in the area and are educated on the subject and are also able to share their knowledge with other stakeholders.
Requirements
- Bachelor’s degree in any field
- A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
- Three (3) years clinical research or related experience
- Advanced knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
- Ability to communicate effectively, both in writing and orally
- Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
- Outstanding customer service skills
- Knowledge of basic human anatomy, physiology medical terminology
- Ability to interpret and master complex research protocol information
- Expert level knowledge of EMR systems, EDC systems, data management systems, statistical software systems (SAS, STATA, R), Patient Outcomes Collection Systems (Patient IQ), research tools (OnCore, RedCap, clinicaltrials.gov, InfoEd), and compliance with institutional regulatory materials.
Nice To Haves
- Bachelor’s degree in science or health related field
- Four (4) years of clinical research or related experience
- Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)
Responsibilities
- Monitor on-going research projects
- Maintain complete records of all research projects
- Track patient study visits and assign duties accordingly
- Assist in design and submission of future research protocols
- Submit and maintain institutional review board for protocols
- Interact with sponsors regarding clinical studies
- Interact with patients during study visits
Benefits
- Medical: Multiple plan options
- Dental: Multiple plan options
- Additional Insurance: Disability, Life, Vision
- Retirement 401(a) Plan: Employer contributes 10%25 of your gross pay
- Paid Time Off: Accruals over the year
- Vacation Days: 22/year (maximum accrual 352 hours)
- Sick Days: 15/year (unlimited maximum accrual)
- Holiday Days: 10/year
- Tuition Benefit: Employees have access to this benefit on all CU campuses
- ECO Pass: Reduced rate RTD Bus and light rail service
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What This Job Offers
Job Type
Full-time
Career Level
Principal
