Clinical Research Pro: Trials, Data & Compliance

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

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.