Research Assistant
Competitive
You'll complete your application on the employer's website.
Competitive
You'll complete your application on the employer's website.
Job type
Salary
Competitive
Location
Sector
Posted
30+ Days Ago
Weill Cornell Medicine is hiring a Research Assistant in its Nuclear Medicine organizational unit. The role supports principal investigators and research coordinators by assisting with clinical study recruitment, data management and analysis, literature reviews, regulatory submissions, and grant documentation.
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
Preferred
Bachelor's degree is preferred
Previous clinical research experience is helpful
Knowledge of medical terminology is helpful
Bachelor's Degree
Clinical Research
Medical Terminology
Company
Academic medical institution providing patient care, research, and physician education
New York, New York, USA
https://careers.weill.cornell.edu/
Founded in 1898
5001-10000 employees
Qualifications
High School Diploma
Approximately one year of related experience
Statistical and database management experience, including proficiency in SPSS and/or RedCap
Standard office work
Bachelor's degree is preferred
Previous clinical research experience is helpful
Knowledge of medical terminology is helpful
Approximately one year of related experience.
Required skills
Statistical Analysis, Database Management, SPSS, REDCap, Clinical Research, Medical Terminology, Qualitative Coding, Thematic Analysis, Institutional Review Board (IRB) Submissions
Preferred skills
Bachelor's degree is preferred, Previous clinical research experience is helpful, Knowledge of medical terminology is helpful, Glassdoor, 3.8, New York, New York, USA, https://careers.weill.cornell.edu, H1B Sponsorship, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, 71, Represents job field similar to this job, Engineering and Development, Education and Training, Customer Service and Support, Management and Executive, Legal and Compliance, Accounting and Finance, Marketing, Trends of Total Sponsorships, *2026, (146), 2025, (171), 2024, (201), 2023, (198), 2022, (151)
Experience
1+ years
Interested in this role?
Apply directly on the employer's website — it only takes a few minutes.
Other roles in New York, NY or Science & Pharmaceutical
Competitive
You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…
When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.
$21.64 - $26.50
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.