Hybrid Clinical Trials Coordinator Associate

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; Hybrid; USD 45,000 - 69,000; Full time

Benefits offered by this job

Relocation assistance

Paid training

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support data collection and the coordination of clinical trials, generally non-therapeutic in nature. You will obtain informed consent, handle specimens and ensure data entry aligns with protocol requirements.

This pre-entry role provides a path toward the Clinical Trials Coordinator career track, with semi-routine duties, moderate supervision, relocation assistance, paid training, and a hybrid on-site/remote work

Qualifications

• Associate’s degree required.
• In lieu of an associate’s degree, 2 years of relevant experience with a high school diploma or GED.
• Bachelor’s degree preferred in scientific, health related or business administration program.

Responsibilities

• Coordinate clinical trials data collection and study procedures.
• Obtain informed consent from participants and assist with specimen collection.
• Perform data entry and assist with regulatory documentation and sponsor communications.
• Support follow-up of patients per protocol and maintain study records.

Skills

Effective communication

Teamwork

Time management

Decision making

Education

Associate's degree

Bachelor's degree preferred

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support data collection and the coordination of clinical trials, generally non-therapeutic in nature. You will obtain informed consent, handle specimens and ensure data entry aligns with protocol requirements.

This pre-entry role provides a path toward the Clinical Trials Coordinator career track, with semi-routine duties, moderate supervision, relocation assistance, paid training, and a hybrid on-site/remote work