Job Description:

Provides assistance to a research staff by collecting data, keeping records, conducting literature searches, technical research, analyzing data, and preparing reports with minimal supervision.

Duties:

• Participates in clinical research projects collecting data from patients and/or participants in a study.


• Collects various forms of data pertaining to the research project or projects, which could include database information and/or hard files.


• Conducts data analyses, interprets data, draws conclusions, and discusses with principal investigator.


• Keeps detailed logs of all research-related projects or activities.


• Prepares various reports containing descriptive, analytical, and evaluative content that may be submitted for publication.


• May assist with the collection of data for internal chart review projects to include collecting data from other sites.


• Assists with the preparation of research charts for clinical and research teams and study-specific reports and queries for investigators and administrators.


• Collaborates with other researchers or colleagues.


• Participates in meetings and presents research findings to fellow researchers and Principal Investigator.


• Assists with audits of study patient documents to identify protocol non-compliance and reports deficiencies to supervisor.


• Performs various duties as needed to successfully fulfill the function of the position.

Required Education: Bachelor's Degree in a Biological Science, Chemistry, or Physical Science or related field, AND

• 12 months research experience.

Equivalency/Substitution: Will accept 48 months equivalent experience in lieu of the Bachelor's Degree for a total of 60 months research experience.

Skills:

• Working knowledge of how to safely handle and dispose of biohazardous materials or chemicals following Federal, State, and University regulations and guidelines.


• Detail oriented.


• Ability to analyze data and keep records.


• Ability to communicate verbally and in writing.

Working Conditions:

• 
  Physical: Standing for prolonged periods. Manual dexterity. Ability to lift up to 25 pounds. Reaching, bending, and stooping.


• 
  Environmental: Laboratory Environment. Exposure to biohazardous materials, chemicals, odors, and/or carcinogens.

Departmental Preferences:

• Experience in a clinical research setting.


• Experience with IRB applications and reviews.


• Previous clinical study experience.


• Database and Redcap knowledge.

Why You Belong at the University of Oklahoma: The University of Oklahoma fosters an inclusive culture of respect and civility, belonging, and access, which are essential to our collective pursuit of excellence and our determination to change lives. The unique talents, perspectives, and experiences of our community enrich the learning, and working environment at OU, inspiring us to harness our innovation, creativity, and collaboration for the advancement of people everywhere.

Equal Employment Opportunity Statement: The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate based on race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures. This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides. 

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