Senior Oncology CRC - Lead Studies & Optimize Operations

Cancer Center of South Florida; Florida; On-site; USD 85,000 - 110,000; Full time

Job summary

The Clinical Research Coordinator III (CRC 3) is a senior-level clinical research professional responsible for independently coordinating and managing complex clinical research studies while ensuring compliance with regulatory, protocol, and institutional requirements.

In addition to overseeing study conduct and participant management, the CRC 3 serves as a team leader and subject matter expert who contributes to process improvement initiatives and supports the development of high-quality

Qualifications

• Bachelor's degree in science, healthcare, or related field.
• Six years direct clinical research experience, including four years oncology.
• Extensive knowledge of medical terminology and clinical research practices.
• Thorough understanding of GCP and HIPAA and applicable regulatory guidelines.

Responsibilities

• Independently coordinate and manage clinical research studies from participant screening through study completion.
• Assess potential research participants for protocol eligibility with PI teams.
• Obtain and document informed consent and ensure ongoing protocol compliance.
• Coordinate and conduct study visits, including specimen collection, processing, storage, shipment, and documentation.
• Collect, enter, maintain, and validate clinical research data in study databases and data collection systems.
• Collaborate with regulatory personnel to ensure regulatory documents are current and complete.

Skills

Clinical research coordination

Oncology research

Regulatory compliance

Data management

Leadership

Mentoring

Documentation

GCP/HIPAA compliance

Education

Bachelor's degree in science/healthcare/related field

Tools

Microsoft Office

Electronic data management systems

Job description

The Clinical Research Coordinator III (CRC 3) is a senior-level clinical research professional responsible for independently coordinating and managing complex clinical research studies while ensuring compliance with regulatory, protocol, and institutional requirements.

In addition to overseeing study conduct and participant management, the CRC 3 serves as a team leader and subject matter expert who contributes to process improvement initiatives and supports the development of high-quality