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About the Role
Provides research, data analysis, and operational support to principal investigators and research coordinators for clinical research studies.
Responsibilities
- Coordinates the recruitment and enrollment of study participants.
- Assesses patient eligibility for inclusion in clinical trials.
- Ensures proper consent protocols have been followed for study participation.
- Assists with departmental mailings, including patient medical records.
- Ensures accuracy of recipient contact information and location for correct delivery.
- Conducts literature reviews and gains expert familiarity with protocols.
- Assists in the creation of study databases.
- Manages and enters collected data into study databases.
- Conducts qualitative coding and thematic analysis of study data.
- May perform statistical analysis of research data.
- Assists in the preparation of materials, submissions, and renewals to the Institutional Review Board (IRB) or IACUC.
- Assists faculty in the preparation of grant submissions and associated documentation.
- Performs other related duties as directed.
Requirements
- Approximately one year of related experience.
Skills
- Statistical and database management experience
- Proficiency in SPSS and/or RedCap
- Previous clinical research experience is helpful
- Knowledge of medical terminology is helpful
Experience Level
- One year of related experience
Education Level
- High School Diploma
- Bachelor's degree is preferred