PS Research Assistant/Analyst

$25,002 - $44,283/Yr

University of Utah - Salt Lake City, UT

posted 2 months ago

Part-time - Entry Level
Salt Lake City, UT
Educational Services

About the position

The Obstetrics & Gynecology Research Network at the University of Utah is seeking a dedicated Research Assistant/Analyst to support a variety of research projects focused on women's and newborn's health. This role involves working closely with investigators, study coordinators, and clinic teams to implement research protocols effectively. The successful candidate will be responsible for conducting internal chart reviews and participating in large-scale studies funded by industry and federal sources. This position is integral to the research team, ensuring that all protocols are followed with precision and that participant safety is prioritized throughout the research process. In this role, the Research Assistant/Analyst will learn and understand study protocols, assess their clarity, and ensure the safety of subjects involved. Responsibilities include screening clinic schedules for potential study participants, conducting eligibility screenings, and recruiting and consenting eligible patients. The individual will explain study protocols to physicians, patients, and healthcare providers, ensuring that all parties understand the inclusion criteria and the study's objectives. Data collection is a critical component of this position, requiring the gathering, recording, and entry of data from study participants and medical records into study databases. The candidate will also maintain essential documentation in compliance with FDA, HIPAA, and GCP guidelines. The role requires collaboration with research teams and clinicians to meet enrollment goals and deadlines, as well as the collection and processing of biospecimens and clinical measurements. The Research Assistant/Analyst will assist in packaging and shipping samples, report and track adverse events, and document any protocol deviations. Participation in team meetings and maintaining supplies will also be part of the job. The work environment is supportive and inclusive, emphasizing teamwork and communication to address any challenges that arise during the research process.

Responsibilities

  • Learn study protocols; assess for clarity and subject safety
  • Review and understand inclusion/exclusion criteria
  • Screen clinic schedules for potential study participants and healthy control participants
  • Carry out study eligibility screening of patients in a clinical setting
  • Recruit and consent eligible patients
  • Explain the study protocol and inclusion criteria to physicians, patients, and health care providers in person and by phone; ensure participant understanding of the protocol
  • Gather, record and enter data from study participants, charts, and EMR's into study databases
  • Maintain source documents, status reports, progress notes, and subject logs in accordance with FDA, HIPAA, and GCP guidelines
  • Complete medical chart reviews
  • Work with research teams and clinicians to meet enrollment goals and study deadlines
  • Collect and process biospecimens and clinical measurements from study participants (phlebotomy training will be provided as needed)
  • Assist in packaging and shipping of samples/biospecimens
  • Report and track adverse events
  • Document all protocol deviations, reconcile test article accountability at study close and prepare summary report for department and sponsor
  • Attend team and study meetings
  • Assist in maintaining stocks of supplies
  • Work with confidential health information and complete the necessary trainings to do so
  • Regulatory management and reporting
  • Other duties as assigned

Requirements

  • Bachelor's degree in a Social or Behavioral Science, Liberal Arts, or a field related to the area of research, or equivalency (one year of education can be substituted for two years of related work experience)
  • One year of experience in research and analytical techniques
  • Demonstrated statistical and quantitative analysis experience
  • Demonstrated human relation and effective communication skills
  • Must fulfill all associated requirements for patient-sensitive position

Nice-to-haves

  • Familiarity with clinical research and study protocols
  • Prior experience interacting with patients in a clinical setting
  • Experience working in women's health
  • Phlebotomy certification
  • Experience with biospecimen collection and processing
  • Prior CITI, HIPAA, GCP and/or IATA training
  • Familiarity with REDCap
  • A background in nursing, science, or a related field

Benefits

  • 401(a)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Retirement plan
  • Vision insurance
  • Wellness program
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