Research Professional 1 - Military Veterans

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