Clinical Trials Coordinator

St. Joseph's Health • Paterson, NJ

1d

About The Position

Under general supervision, coordinates clinical research protocols; interacts with sponsors, investigators, data coordinating centers, and core laboratory personnel as needed; ensures that the regulatory binders are complete and up-to-date; executes and adheres to the clinical trial research protocols; performs follow-up procedures and completes case report forms; prepares documents for IRB submission in compliance with all local, state, and federal regulations. Screens potential research patients for clinical research protocols and gathers data while maintaining patient confidentiality.

Requirements

• Work requires the knowledge of theories, principles, and concepts normally acquired through completion of a Associates degree in Business, Public Health, or Health Education, and one to three years of previous work related experience.

Nice To Haves

• SOCRA certification preferred
• Patient Care Associate Adult Phlebotomy certification preferred
• Previous experience in clinical research or clinical trials coordination program management preferred.

Responsibilities

• coordinates clinical research protocols
• interacts with sponsors, investigators, data coordinating centers, and core laboratory personnel as needed
• ensures that the regulatory binders are complete and up-to-date
• executes and adheres to the clinical trial research protocols
• performs follow-up procedures and completes case report forms
• prepares documents for IRB submission in compliance with all local, state, and federal regulations
• Screens potential research patients for clinical research protocols and gathers data while maintaining patient confidentiality.

What This Job Offers

• Job Type: Full-time
• Education Level: Associate degree