Clinical Research Associate

Touro University is a healthcare institution seeking a Clinical Research Associate. The role involves managing clinical trial processes, ensuring compliance with regulations, and collaborating with clinical teams for patient enrollment and data management.

Responsibilities

• Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team
• Assist in new IRB application and annual renewal process of COG, sponsored, local and other multi-institutional protocols
• Screen and enroll patients onto clinical trials in collaboration with clinical team, ensure protocol compliance; coordination of specimen collection and transmittal in collaboration with clinical team
• Ensure compliance with the Good Clinical Practice guidelines in clinical research
• Monitor study patients for adverse events in collaboration with clinical team and report as required
• Enter data on Hematology, Oncology and Stem Cell Transplant patients on electronic data capture forms; prepare for routine data audits and maintain source documents and regulatory binders
• Manage communications- mail, phone, fax, e-mail for COG, sponsored, local and multi-institutional studies
• Act as liaison between NYMC and Westchester Medical Center, regarding new study requirements

Company

• Jewish-sponsored independent institution of higher and professional education
• New York, New York, USA
• https://www.touro.edu/
• Founded in 1970
• 1001-5000 employees

Qualifications

• BS
• Must have a keen attention to detail
• Be able to multi-task and prioritize assignments
• Touro University is a higher education organization focused on the Jewish community.
• New York, New York, USA
• https://www.touro.edu
• H1B Sponsorship
• Data Powered by
• Distribution of Different Job Fields Receiving Sponsorship
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• Engineering and Development
• Education and Training
• Customer Service and Support
• Management and Executive
• Trends of Total Sponsorships
• *2026
• (7)
• 2025
• (11)
• 2024
• (5)
• 2023
• (8)
• 2022
• (1)
• Late Stage
• Leadership Team
• Mike Newman
• Senior Vice President, General Counsel & Chief Compliance Officer
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Required skills

• Adverse event management, Clinical Practice, Clinical trial protocol compliance, Data collection and management, Electronic data capture, IRB application process, Regulatory submission, Specimen collection and transmittal, Subject screening and enrollment

Experience

• Mid level