Clinical Research Associate

Touro University; Hawthorne (NY); On-site; USD 48,000 - 60,000; Full time

Job summary

Touro University is seeking a dedicated individual for a role involving the management of clinical trial activities, including patient enrollment and regulatory submissions. The ideal candidate has a BS and skills in attention to detail and multi-tasking.

Responsibilities include assisting with IRB applications, ensuring compliance with Good Clinical Practice, and managing data entry for studies in the New York area.

The position offers a salary range of $48,000 to $60,000 annually.

Qualifications

• BS required.
• Must have keen attention to detail and strong organizational skills.

Responsibilities

• Assist in new IRB application and annual renewals.
• Screen and enroll patients onto clinical trials.
• Ensure compliance with Good Clinical Practice guidelines.
• Monitor study patients for adverse events.
• Manage data entry and communication for studies.

Skills

Attention to detail

Multi-tasking

Prioritization skills

Education

Bachelor of Science

Job description

Overview

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.

Responsibilities

• 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 the clinical team, ensure protocol compliance; coordination of specimen collection and transmittal in collaboration with the clinical team.
• Ensure compliance with the Good Clinical Practice guidelines in clinical research.
• Monitor study patients for adverse events in collaboration with the 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.

Qualifications

Education requirement: BS

Other skills/requirements: Must have a keen attention to detail, be able to multi-task and prioritize assignments.

Salary

Minimum: USD $48,000.00/Yr.

Maximum: USD $60,000.00/Yr.