Research Assistant (Evenings/Weekends)

Weill Cornell Medicine - New York, NY

Full-time

New York, NY

Educational Services

About the position

The Research Assistant position at Moeun Son Lab is designed for individuals who are eager to contribute to clinical research studies under the guidance of principal investigators and research coordinators. This role is particularly focused on providing essential research, data analysis, and operational support, which are critical for the successful execution of clinical trials. The position requires a commitment to working evenings and weekends, aligning with the needs of the research team and study participants. The Research Assistant will play a vital role in coordinating the recruitment and enrollment of study participants, ensuring that all protocols are adhered to, and that the integrity of the research is maintained throughout the process. In this role, the Research Assistant will be responsible for assessing patient eligibility for inclusion in clinical trials, which involves a thorough understanding of the study protocols and the ability to communicate effectively with potential participants. The position also entails managing departmental mailings, including the handling of patient medical records, ensuring that all contact information is accurate for proper delivery. The Research Assistant will conduct literature reviews to gain familiarity with the protocols that will be utilized as templates for the studies, which is essential for maintaining high standards of research quality. Additionally, the Research Assistant will assist in the creation and management of study databases, entering collected data accurately and conducting qualitative coding and thematic analysis of the study data. There may also be opportunities to perform statistical analysis of research data, contributing to the overall findings of the studies. The role includes assisting faculty with the preparation of materials for submissions and renewals to the Institutional Review Board (IRB) or IACUC, as well as supporting grant submissions and related documentation. Overall, this position is integral to the research team, providing a foundation for successful clinical research outcomes.

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 that will be used as templates.
• Assists in creation of study database.
• Manages and enters collected data into study database.
• 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, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts.
• Performs other related duties as directed.

Requirements

• High School Diploma required; Bachelor's degree preferred.
• Approximately one year of related experience.
• Statistical and database management experience, including proficiency in SPSS and/or RedCap.
• Previous clinical research experience is helpful.
• Knowledge of medical terminology is helpful.