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Data Entry Research Assistant

Data Entry Research Assistant (Temporary Aide)
Division of Pulmonary Sciences and Critical Care Medicine
Job Summary
Temporaries perform seasonal, temporary work for short periods of time (e.g., summer months, special events, or projects) and are exempt from the state classified system based on 100% funding from gifts, grants or auxiliaries. Positions have limited duration work assignments in accordance with university or campus policies and are not part of the regular staffing pattern for the organization. Appointments are limited to 9 months of continuous employment with a 4 month break OR 9 months of employment in any 12 month period.
Nature of Work: 
The Division of Pulmonary Sciences and Critical Care Medicine is seeking an organized individual for a temporary, part-time position (20 hours/week during the summer months) to help the Asthma Research Team in performing research related tasks. Due to COVID precautions, this part-time position can be done completely remotely. This Data Entry Research Assistant position will be responsible for data entry, regulatory compliance, and assisting research coordinators in duties associated with performing clinical research activities. Hours of work will be dependent on workload but estimated to be 15-20 hours a week.
Duties and Responsibilities: 
The successful candidate will be a productive member of the research team, participate in research projects, and help maintain the databases of several studies. The candidate should be able to work independently and as a member of a team. Flexible work hours, including infrequent evenings or weekends, may be required. Candidate will work closely with the Principal Investigators and the study team in a cooperative environment. Excellent communication skills, the ability to multitask, along with orientation toward teamwork and cooperation are required. The applicants should demonstrate that they are well organized, reliable, independent, and possess considerable attention to detail. They should also have excellent verbal, written, and computational skills.
Examples of Work Performed:
·      Complete electronic medical records (EPIC) queries to complete data entry requirements
·      Completes data entry using various data electronic capturing systems (REDCAP, Access, Medidata, etc)
·      Adherence to and technical knowledge of regulatory compliance issues related to human subjects research
·      Participate in staff in-service trainings on study protocols, team and divisional staff meetings
·      Work closely with the Principal Investigators and study staff regarding database management
·      Attend trainings as necessary for required credentials
·      Willingly accepts additional responsibilities and duties as assigned by management
·      Other duties as assigned
Supervision Received: 
The Data Entry Research Assistant will be supervised by and will report to the Program Manager and 2 Principal Investigators
Supervision Exercised: 
This position pays $15/hour for up to 20/hours a week
Diversity and Equity
Please click here for information on disability accommodations:
The University of Colorado Denver | Anschutz Medical Campus is committed to recruiting and supporting a diverse student body, faculty and administrative staff. The university strives to promote a culture of inclusiveness, respect, communication and understanding. We encourage applications from women, ethnic minorities, persons with disabilities and all veterans. The University of Colorado is committed to diversity and equality in education and employment.

Minimum Qualifications:
·      Associate of Arts degree or equivalent
·      Must be able to meet credentialing requirements at area hospitals
·      Some research experience
Required Competencies/Knowledge/Skills/Abilities:
·      Ability to prioritize numerous tasks and complete them under strict time constraints
·      Good interpersonal, organizational, and communication skills
·      Proficient with computers and Microsoft office software, computer data entry, and data management
·      Ability to follow detailed and complicated protocols
·      Ability to be team oriented and flexible
·      Ability to work independently with minimal supervision
 Desired Qualifications:
·      Prior clinical research experience
·      Knowledge of GCP/ICH guidelines and human subjects research
·      Experience with patient-oriented research
·      Experience with electronic data capture systems (REDCAP, OnCore)