Senior Oncology CTMS Analyst (Contract)
Location: Miami, FL
Contract (15 Weeks)
Schedule: Monday – Friday | 8:30 AM – 5:00 PM
Pay: $28.00 – $38.00 per hour

An established hospital in the Miami area is seeking an experienced Senior Oncology CTMS Analyst for a 15-week contract assignment. This role is ideal for a healthcare IT or clinical research professional with strong experience supporting Clinical Trial Management Systems (CTMS), oncology research operations, and end-user support.
If you have a passion for improving clinical research workflows through technology and enjoy collaborating with multidisciplinary teams, we'd like to hear from you.

Responsibilities
• Support the implementation, configuration, maintenance, and optimization of the Clinical Trial Management System (CTMS).
• Serve as the primary analyst for oncology clinical research workflows and CTMS functionality.
• Analyze business processes and recommend system enhancements to improve efficiency and compliance.
• Collaborate with clinical research staff, investigators, IT teams, and vendors to resolve system issues.
• Perform system testing, validation, troubleshooting, and quality assurance activities.
• Develop reports, dashboards, and data extracts to support research operations and regulatory requirements.
• Create and maintain system documentation, workflows, and user guides.
• Provide training and ongoing support to CTMS users.
• Ensure data integrity and compliance with institutional policies and regulatory requirements.

Qualifications
• Bachelor's degree in Information Systems, Healthcare Administration, Clinical Research, or a related field preferred.
• 3+ years of experience supporting a Clinical Trial Management System (CTMS).
• Experience working in oncology clinical research within a hospital, academic medical center, or healthcare environment.
• Strong understanding of clinical trial operations, research workflows, and regulatory requirements.
• Experience with system configuration, testing, reporting, and user support.
• Excellent analytical, problem-solving, and communication skills.
• Ability to manage multiple priorities in a fast-paced environment.

Preferred Qualifications
• Experience with OnCore CTMS or other enterprise Clinical Trial Management Systems.
• Knowledge of clinical research regulations, GCP, and oncology research protocols.
• Experience working with EHR integrations and clinical research reporting tools.

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