Job Title: Clinical Research Coordinator

Job Description

We are seeking a dedicated Clinical Research Coordinator to join our prestigious academic research institute. This role involves recruiting, screening, and enrolling subjects into clinical trials, explaining the informed consent process, documenting adverse events, and collecting essential study documents. The coordinator will also be responsible for preparing Institutional Review Board applications, supporting CAR-T sponsor drug trials, and being part of starting up new studies.

Responsibilities

• Recruit, screen, and enroll subjects into clinical trials.
• Explain the informed consent process to participants.
• Document adverse events as they occur during trials.
• Collect study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.
• Prepare Institutional Review Board (IRB) applications.

Essential Skills

• Enrollment and informed consent process knowledge.
• Experience in patient oncology research.
• Proficiency in clinical research coordination and data entry.
• Ability to conduct chart reviews and understand regulatory requirements.
• Experience in patient recruitment and consenting.
• Effective communication and writing skills.
• Knowledge of IRB and human research protection regulations.

Additional Skills & Qualifications

• Bachelor's degree (BA/BS) preferred.
• 1-3 years of clinical research experience required.
• Experience with in-hospital clinical research.
• Experience with adverse event reporting.

Work Environment

The role involves working in a combination of office and hospital/outpatient surgery settings, within a very fast-paced and high-volume workload environment. You will be part of the largest team at the cancer center, with ample support, working on high-profile studies with large, well-known sponsors. The institute is equipped with state-of-the-art facilities, and the position offers the opportunity to work on industry-leading and investigator studies.