Clinical Research Coordinator Associate

About the role

The Clinical Research Coord. Associate (CRC Assocc.) supports clinical research at Moffitt Cancer Center. This position involves coordinating non-therapeutic research protocols, obtaining informed consent, collecting specimens, and entering data.

Responsibilities

• Obtain informed consent from study participants
• Coordinate specimen collection
• Enter data into various database systems
• Follow up with patients according to protocol
• Order supplies and prepare patient documents
• Maintain regulatory documents
• Communicate with study sponsors
• Facilitate the collection of study-required specimens

Requirements

Requires a high school diploma or equivalent. Previous experience in a clinical research setting is preferred but not required. Must have strong organizational and communication skills, and be able to work independently and as part of a team.

Qualifications

Must be able to pass a background check and drug screen. Must be able to work flexible hours, including evenings and weekends. Must have a valid driver’s license and reliable transportation.

Skills

Strong attention to detail, excellent communication skills, ability to work independently and as part of a team, proficiency in Microsoft Office, and knowledge of Good Clinical Practice (GCP) guidelines.

Benefits

Moffitt offers a comprehensive benefits package including health insurance, dental insurance, vision insurance, retirement plans, paid time off, and more. Employees also have access to wellness programs and continuing education opportunities.

Pay

Salary range: $40,000 - $60,000 annually. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

Schedule

The Clinical Research Coord. Associate works a flexible schedule, including evenings and weekends, to accommodate the needs of the research protocols they support.