Research Assistant

Weill Cornell Medicine - Qatar; New York (NY); On-site; USD 52,000 - 72,000; Full time

Job summary

Weill Cornell Medicine - Qatar is seeking a detail-oriented research assistant to support clinical studies. You will assist researchers with data collection, literature reviews, and protocol development, coordinating participant recruitment and data entry.

The role requires familiarity with medical terminology, SPSS or REDCap, and an ability to handle multiple tasks in a fast-paced research environment. Bachelor's degree is preferred, with about one year of related experience.

Qualifications

• Bachelor's degree is preferred.
• Approximately one year of related experience.
• Experience with SPSS or REDCap is preferred.
• Knowledge of medical terminology is helpful.

Responsibilities

• Coordinate the recruitment and enrollment of study participants and assess eligibility.
• Assist with departmental mailings and patient records. Ensure accuracy of recipient contact information and location.
• Conduct literature reviews and gain familiarity with protocols used as templates.
• Assist in creation of study database and manage data entry.
• Enter and manage data in study databases.
• Conduct qualitative coding and thematic analysis of study data.
• May perform statistical analysis of research data.
• Assist in IRB/IACUC submissions and renewals.
• Assist with grant submissions and related documents.
• Perform other related duties as directed.

Skills

Statistical analysis

Data analysis

Clinical research

Education

High School Diploma

Bachelor's degree preferred

Tools

SPSS

REDCap

Job description

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*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Position Summary

Under direction, provides research, data analysis and operational support to principal investigators and research coordinators for clinical research studies

Job 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.

Education

• High School Diploma

Experience

Bachelor's degree is preferred.

Approximately one year of related experience.

Knowledge, Skills and Abilities

• Statistical and database management experience, including proficiency in SPSS and/or RedCap.
• Previous clinical research experience is helpful.
• Knowledge of medical terminology is helpful.

Licenses and Certifications

Working Conditions/Physical Demands

Standard office work

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