Clinical Research Coordinator Associate — Cancer Trials

Moffitt Cancer Center; United States; On-site; USD 30,000 - 45,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coord. Associate to support data collection and coordination of clinical trials. This entry-level role involves obtaining informed consent, data entry, and assisting with regulatory documents within oncology research settings.

The position offers semi-structured supervision and clear paths toward Clinical Trials Coordinator roles, with responsibilities spanning data management, specimen handling, and collaboration with sponsors and care teams.

Qualifications

• Associates degree required, in lieu of Associates degree 2 years of relevant experience with a high school diploma or GED.
• Preferred: Hands on research experience preferred with one year experience in the oncology research setting.

Responsibilities

• Assists with data entry into study databases and EMR systems.
• Coordinates activities for assigned research protocols and ensures informed consent is obtained.
• Supports maintenance of regulatory documents and prepares patient/participant documents for visits.
• Communicates with study sponsors and participates in specimen collection per protocol.
• Performs scheduling, follow-up, and ensures data integrity for trial activities.

Skills

Attention to detail

Data entry

Communication

Education

Associates degree or 2 years relevant experience

Job description

Moffitt Cancer Center is seeking a Clinical Research Coord. Associate to support data collection and coordination of clinical trials. This entry-level role involves obtaining informed consent, data entry, and assisting with regulatory documents within oncology research settings.

The position offers semi-structured supervision and clear paths toward Clinical Trials Coordinator roles, with responsibilities spanning data management, specimen handling, and collaboration with sponsors and care teams.