Oncology Clinical Research Coordinator

Job Description

The Oncology Clinical Research Coordinator will be responsible for managing and coordinating clinical trials in oncology. This role involves working closely with investigators, patients, and regulatory personnel to ensure the successful execution of clinical research studies.

Key Responsibilities

• Coordinate and manage oncology clinical trials from initiation to closeout.
• Recruit, screen, and enroll study participants.
• Obtain informed consent from study participants.
• Monitor patient safety and compliance with study protocols.
• Collect, process, enter, and manage clinical data.
• Maintain accurate and complete study documentation.
• Communicate with investigators, sponsors, and regulatory agencies.
• Ensure compliance with all regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Assist in the preparation of study-related documents and reports.
• Provide support during audits and inspections