Clinical Research Assistant: Data, IRB & Grants Support

Weill Cornell Medicine

New York (NY)

On-site

USD 52,000 - 70,000

Full time

2 days ago
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Job summary

Weill Cornell Medicine seeks an organized research support professional to assist principal investigators and coordinators in clinical studies in New York City. You will coordinate recruitment, assess eligibility, and ensure proper consent procedures are followed.

Responsibilities include literature reviews, data entry into study databases, coding and analysis where appropriate, and assisting in grant submissions and regulatory documents. Standard office environment with diverse teams.

Qualifications

  • Statistics and database management experience including SPSS/REDCap.
  • Previous clinical research experience is helpful.
  • Knowledge of medical terminology is helpful.

Responsibilities

  • Coordinates recruitment and enrollment of study participants and assesses eligibility.
  • Assists with departmental mailings and ensures correct delivery of medical records.
  • Conducts literature reviews and gains familiarity with protocol templates.
  • Assists in creation of study database and data entry.
  • Manages and enters data into the study database.
  • Conducts qualitative coding and thematic analysis of study data.
  • May perform statistical analysis of research data.
  • Assists in preparation of IRB/IACUC submissions and renewals.
  • Supports faculty in grant submissions and related documentation.

Skills

Statistical reasoning
Literature review

Education

Bachelor's degree (preferred)
High School Diploma

Tools

SPSS
REDCap

Job description

Weill Cornell Medicine seeks an organized research support professional to assist principal investigators and coordinators in clinical studies in New York City. You will coordinate recruitment, assess eligibility, and ensure proper consent procedures are followed.

Responsibilities include literature reviews, data entry into study databases, coding and analysis where appropriate, and assisting in grant submissions and regulatory documents. Standard office environment with diverse teams.

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