Senior Clinical Research Coordinator – Oncology Studies

Cancer Center of South Florida; Lake Worth (TX); On-site; USD 80,000 - 110,000; Full time

Job summary

The Clinical Research Coordinator III (CRC 3) at Cancer Center of South Florida leads complex oncology studies, ensuring regulatory compliance and data integrity across sites. This senior role coordinates visits, handles consent, and mentors study staff while driving process improvements.

They independently manage study conduct, collaborate with investigators and sponsors, and ensure high-quality clinical research operations while maintaining audit readiness and adherence to GCP, HIPAA, and

Qualifications

• Thorough knowledge of medical terminology and clinical research practices.
• Strong understanding of GCP and HIPAA and applicable regulatory guidelines.
• Ability to interpret study protocols and informed consent requirements.
• Excellent organizational skills to manage multiple studies, priorities and deadlines.
• Attention to detail and commitment to data accuracy and quality.
• Proficiency with MS Office and electronic data management systems.
• Effective verbal and written communication with diverse audiences.
• Leadership, mentoring, and training skills for study teams.

Responsibilities

• Independently coordinate and manage clinical research studies from screening to completion.
• Assess participant eligibility in collaboration with investigators.
• Obtain informed consent and ensure protocol compliance.
• Coordinate and conduct study visits, including specimen handling.
• Enter and validate data in study databases and systems.
• Maintain regulatory documents current and complete with regulatory personnel.
• Ensure compliance with GCP, HIPAA, sponsor requirements, and regulatory standards.
• Perform QA/QC to ensure audit readiness of studies.
• Develop study tools, source documents, workflows, and training materials.
• Collaborate with investigators, sponsors, monitors, and multidisciplinary teams.
• Identify and support new clinical research opportunities.

Skills

Medical terminology

GCP & HIPAA

Study protocol interpretation

Organizational skills

Data accuracy

MS Office / EDC

Communication skills

Leadership & mentoring

Education

Bachelor’s degree in science/healthcare

Job description

The Clinical Research Coordinator III (CRC 3) at Cancer Center of South Florida leads complex oncology studies, ensuring regulatory compliance and data integrity across sites. This senior role coordinates visits, handles consent, and mentors study staff while driving process improvements.

They independently manage study conduct, collaborate with investigators and sponsors, and ensure high-quality clinical research operations while maintaining audit readiness and adherence to GCP, HIPAA, and