Entry Clinical Research Professional - PRA

at  University of Colorado

JOB SUMMARY:

The selected applicant will join an interdisciplinary team of scholars to conduct research examining the ethical, legal and social implications of ingestible electroceuticals, mRNA drug delivery devices and related emerging technologies. The aim of this research is to develop an ethical and regulatory framework for development and use of these groundbreaking therapies.

Key Responsibilities:

• Scoping review protocol development, literature cleaning, data collection, coding, and analysis
• Participant recruitment for interviews and expert panel
• Conducting, coding and analyzing interviews
• Arranging and participating in meetings of internal and external researchers and stakeholders
• Prepare tables and figures for papers, presentations, and other academic products
• Coordinate members of the study team and ensure regulatory compliance
• Prioritize work across multiple studies or deadline
• Contribute to papers, with an opportunity to lead work in a specific area

MINIMUM QUALIFICATIONS:

Applicants must meet minimum qualifications at the time of hire.

• Bachelor’s degree in any field

PREFERRED QUALIFICATIONS:

• A Master’s degree in Bioengineering
• Research team / research project management experience
• Experience working in a bioethics center
• Experience with scoping review methods, such as screening articles for inclusion
• Experience with reviewing diverse types of scientific literature including government reports and websites
• Experience with Qualtrics, PubMed, Covidence, Google Scholar, Web of Science, Embase
• Record of research publication
• Experience organizing and participating in research team meetings and meetings with stakeholders

KNOWLEDGE, SKILLS, AND ABILITIES:

• Excellent written and verbal communication skills
• Proficiency in all Microsoft Office applications (Word, Excel, Outlook, PowerPoint)
• Ability to work on multiple projects simultaneously
• Remain detail-oriented with changing priorities
• Ability to work independently following training
• Customer service-oriented to work with diverse faculty and staff
• Ability to form collaborative and effective working relationships

• Scoping review protocol development, literature cleaning, data collection, coding, and analysis
• Participant recruitment for interviews and expert panel
• Conducting, coding and analyzing interviews
• Arranging and participating in meetings of internal and external researchers and stakeholders
• Prepare tables and figures for papers, presentations, and other academic products
• Coordinate members of the study team and ensure regulatory compliance
• Prioritize work across multiple studies or deadline
• Contribute to papers, with an opportunity to lead work in a specific are