Research Professional 1 - Military Veterans
at HERC- Upper MidWest
60% Independent Trial Management/Coordination as a Subject Coordinator:
- Consent patients to participate in research studies
- Work with providers to determine eligibility for study
- Schedule and coordinate with patients and care team to ensure all procedures are completed according to the research protocol
- Work with sponsor to meet deadlines for enrollment and procedures being completed
40% Data Management:
- Review medical records for data related to study procedures and enter into study database
- Answer queries or quality checks for data entry
- Pull data for statistical analysis and assist with analyzing and interpreting results as needed
All required qualifications must be documented on application materials
Required Qualifications:
Education:
- BA/BS degree or a combination of related education and work experience to equal four years.
Data Management:
- Proven ability to manage and enter data accurately, review sensitive records and maintain confidentiality. Must include proficiency in Microsoft Office and Google Workplace.
Communication and Organizational Skills:
- Experience managing multiple projects and deadlines and effective verbal and written communication skills (i.e. communicating with diverse stakeholders such as clients, team members, and external partners).
Work Environment:
- Ability to work on-site, required to be in the office Monday through Friday, with flexibility based on the OR schedule.
- Willingness to travel to community clinics around the metro area; must have reliable transportation.
- Comfort working in an OR setting and inpatient units.
References from previous employers will be required at time of offer
Preferred Qualifications:
- Healthcare/Clinic experience
- Women's Health Interest
Minneapolis, MN
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