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About the Role
Provides research, data analysis, and operational support to principal investigators and research coordinators for clinical research studies under direction.
Responsibilities
- Coordinate recruitment and enrollment of study participants.
- Assess patient eligibility for clinical trials.
- Ensure proper consent protocols are followed.
- Assist with departmental mailings and medical records management.
- Conduct literature reviews and maintain familiarity with study protocols.
- Assist in the creation and management of study databases.
- Enter collected data into study databases.
- Conduct qualitative coding and thematic analysis of study data.
- Perform statistical analysis of research data.
- Assist in preparation of materials, submissions, and renewals for IRB or IACUC.
- Assist faculty in preparation of grant submissions, progress reports, and manuscripts.
Requirements
- High School Diploma.
- Approximately one year of related experience.
Skills
- Statistical analysis
- Database management
- SPSS
- RedCap
- Clinical research
- Medical terminology
Location
- Upper East Side, NYC
Work Type
- 35 hours per week
- Non-Exempt
Experience Level
- Approximately one year of related experience
Education Level
- High School Diploma
- Bachelor's degree preferred
Salary/Compensations
- $24.29 - $27.09 per hour
About the Company
- Roger Hartl Research
- Cornell University
Equal Opportunity
- Cornell welcomes students, faculty, and staff with diverse backgrounds and prohibits discrimination based on any legally protected status.
- Cornell engages in affirmative action in employment for qualified protected veterans and qualified individuals with disabilities.