Clinical Research Coordinator II - GYN

Summary

Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center focused on the prevention and cure of cancer. The Clinical Research Coordinator II supports principal investigators in coordinating clinical trials, including patient screening, enrollment, care coordination, documentation, and protocol compliance. The role serves as a liaison among investigators, care providers, regulatory staff, and study sponsors while managing moderately complex studies.

Responsibilities

• Supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center
• Supporting PI sponsored IND or IDE trials
• Coordinating patient care by collaborating with medical staff, and documenting in accordance with standards and regulatory guidelines
• Acting as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor
• Screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
• Performing all CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I
• Determining methods and procedures for the coordination of newly assigned studies

Skills

• Two (2) years of clinical trials coordination experience
• *Associate's degree considered with two (2) additional years of experience.*
• TheCRC II is required to have thorough knowledge of word processing (Microsoft Office Suite), data base entry, and thorough knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research
• They should be proficient in the use of EMR systems, clinical trial management systems and various other data capture/reporting systems
• This person must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals
• A proficient understanding of medical terminology required
• The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing
• The ability to prioritize assignments and pace one's-self when working under the pressure of deadlines and work volume is required
• Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred
• CCRP/CCRC or equivalent preferred

Qualifications

Must Haves

• Two (2) years of clinical trials coordination experience
• *Associate's degree considered with two (2) additional years of experience.*
• TheCRC II is required to have thorough knowledge of word processing (Microsoft Office Suite), data base entry, and thorough knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research
• They should be proficient in the use of EMR systems, clinical trial management systems and various other data capture/reporting systems
• This person must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals
• A proficient understanding of medical terminology required
• The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing
• The ability to prioritize assignments and pace one's-self when working under the pressure of deadlines and work volume is required

Nice to Haves

• Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred
• CCRP/CCRC or equivalent preferred

Benefits

• Monday through Friday schedule
• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period
• Paid training and orientation through its CTO (Clinical Trails Office) Academy
• Relocation assistance may be provided