OPEN RANK Research Services Intermediate or Senior Professional

University of ColoradoAurora, CO
Onsite

About The Position

The C3 Global Trauma Network conducts innovative, collaborative, federally-funded trauma care research, primarily in high-trauma international settings. It employs rigorous observational and interventional methodologies to address contemporary clinical knowledge gaps, aiming to generate high-quality evidence to enhance early trauma (injury) care, with a specific focus on improving patient outcomes in resource-constrained environments like South Africa. The network has a strong record of NIH and U.S. Department of Defense funding, numerous peer-reviewed publications, and scientific presentations, striving to fill clinical and scientific gaps for civilians globally and the U.S. military. The successful candidate will join a highly collaborative and exciting multi-disciplinary team, located in both the USA and South Africa, as a Research Services Professional. Intermediate Clinical Science Professionals perform clinical research functions, including patient-oriented research or research with human subjects, focusing on mechanisms of human disease, therapeutic interventions, clinical trials, or the development of new technologies. They may also contribute to epidemiologic and behavioral studies, outcomes research, and health services research. Senior Clinical Science Professionals perform similar clinical research functions, with the understanding that some assignments may not progress beyond this level. The level of responsibility, technical complexity, and autonomy for the Research Services Professional will increase in accordance with their job tier (intermediate or senior).

Requirements

  • Bachelor’s degree in any field OR a combination of education and related technical/paraprofessional experience (may be substituted for the bachelor’s degree on a year for year basis)
  • One (1) year clinical research or related experience (for Intermediate Professional)
  • Two (2) years clinical research or related experience (for Senior Professional)
  • 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
  • Demonstrated commitment and leadership ability to advance diversity and inclusion
  • Knowledge of basic human anatomy, physiology medical terminology
  • Ability to interpret and master complex research protocol information
  • Familiarity with medical/research terminology, medical charts, and research regulatory requirements
  • Ability to think creatively, adapt quickly, and work independently
  • Excellent team player and contributor to the larger goals of the research from an operational level
  • Enjoys working with data relating to human research subjects
  • Self-starter with a desire to improve human health through research
  • High Level Skills with Computer-Based Tools (Word, Outlook, PowerPoint, etc.)
  • Applicants must be legally authorized to work in the United States without requiring sponsorship

Nice To Haves

  • Two (2) years of clinical research or related experience for intermediate and Three (3) years of clinical research or related experience for senior
  • Relevant Master’s degree in research-related discipline (may be substituted for experience on a year for year basis if the degree is in a field of study directly related to the work assignment)
  • Previous experience working in global health, emergency care, or trauma-related research
  • Clinical or health-related research experience, including data management or data quality control
  • Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)
  • Experience with and understanding of medical terminology
  • Experience in an emergency department, prehospital (i.e., ambulance), or inpatient setting
  • Experience preparing and submitting scientific manuscripts to peer-reviewed health journals
  • Skills with REDCap (creating forms, running reports, exporting datasets)

Responsibilities

  • Working closely with a research team domestically and internationally
  • Data organization and quality
  • Data collection instrument development and maintenance
  • Data description/summarization/analysis
  • Manuscript development
  • Creating stakeholder presentations
  • Preparing abstracts and presentations for medical conferences

Benefits

  • Medical: Multiple plan options
  • Dental: Multiple plan options
  • Additional Insurance: Disability, Life, Vision
  • Retirement 401(a) Plan: Employer contributes 10% 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
  • Many additional perks & programs with the CU Advantage
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