Research Services Entry Professional

University of ColoradoColorado Springs, CO
$24 - $31Hybrid

About The Position

Entry 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. Entry Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. This role will support human subjects research studies conducted within the Rehabilitation and Biomechanics (RAB) Laboratory. Responsibilities include participant recruitment and scheduling, laboratory operations, assistance with biomechanical data collection, data management, literature review, and assistance with dissemination of research findings. Current projects include NIH-funded studies investigating dynamic joint stability and musculoskeletal function in individuals with generalized joint hypermobility.

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.
  • Applicants must meet minimum qualifications at the time of hire.
  • Applicants must be legally authorized to work in the United States without requiring sponsorship.
  • 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
  • Problem-solver, strong analytical and technical skills
  • Demonstrated organizational and project management skills
  • Ability to work independently, solve problems, and take initiative to ask for help when appropriate
  • Attention to detail and accuracy in data collection and record keeping.
  • Ability to manage multiple priorities and meet deadlines.
  • Ability to learn new research methods, equipment, and software applications.
  • Ability to work effectively with participants from diverse backgrounds.

Nice To Haves

  • BS in engineering, kinesiology, or physiology.
  • Clinical research or related experience.
  • Experience with electronic data capture systems (e.g. EMR or EHR and data management systems).
  • Experience working in a biomechanics lab (optical motion capture, isokinetic dynamometer, force plates)
  • Coding experience (MATLAB, python)

Responsibilities

  • Assist with and oversee the day to day operations of clinical trials and studies
  • Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial
  • Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required
  • Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies through phone contacts and personal interviews
  • Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
  • Collect, code, and analyze data obtained from research in an accurate and timely manner
  • Adhere to research regulatory standards
  • Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
  • Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
  • Ensure that the necessary supplies and equipment for studies are in stock and in working order
  • Assist with integration of equipment and software, and troubleshooting technical aspects of data collection.
  • Maintain laboratory equipment, supplies, and testing spaces to support ongoing research activities.
  • Coordinate with other research teams sharing equipment and lab space.
  • Assist with development, implementation, and revision of research protocols and study procedures.
  • Assist with organizing documentation and data collection materials.
  • Operate research equipment including motion capture systems, force plates, dynamometers, load cells, electromyography systems, and other laboratory instrumentation.
  • Prepare participants and testing environments, collect study data according to established protocols, and document testing procedures.
  • Schedule and communicate with research participants for ongoing research studies.
  • Coordinate participant visits and monitor study activities to support successful completion of research projects.
  • Enter, organize, and verify research data within study data management systems.
  • Assist with data preparation and organization for analysis, reporting, and dissemination activities.
  • Conduct literature searches and summarize scientific evidence relevant to ongoing research projects.
  • Participate in research team meetings and contribute to project planning activities.
  • Assist with preparation of abstracts, scientific presentations, posters, manuscripts, and research reports.
  • Perform other research-related duties and special projects as assigned.

Benefits

  • Generous leave
  • Health plans
  • Retirement contributions
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