Moffitt Cancer Center

SPVR CLINICAL TRIALS OFFICE


PayCompetitive
LocationTampa/Florida
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: 70663

      At Moffitt Cancer Center, we come face-to-face with cancer every day, but we also see courage. And it inspires us to be the safest and best place for cancer care – to bring greater hope to every patient we serve. It’s why we’ve been continually named One of the Top Places to Work in the Tampa Bay Area. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Moffitt is the leading cancer hospital in both Florida and the Southeast and has been nationally ranked by U.S. News & World Report since 1999. Because working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join a dedicated, diverse and inclusive team of over 7,000 to be a part of the Courageous future we envision.

      Summary

      Position Highlights:

      • Provides basic day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible CTO manager and in collaboration with faculty and investigators.
      • Works effectively across the organization and externally with sponsor organizations to ensure effective and efficient conduct of clinical research.
      • Supports the recruiting, training, development, and performance management of assigned staff.
      • Operationally focuses on study start up, trial coordination, and quality assurance needs, providing problem-solving and troubleshooting expertise.
      • Will be expected to identify process improvement opportunities, collaborate with their team to develop creative solutions, lead/delegate implementation, and track success through defined metrics.

      Responsibilities:

      • Provide daily supervision of research staff including scheduling to meet program business needs and orientation and training.
      • Supervise the staff responsibilities for the clinical aspects of study start up.
      • Serve as resource to investigators writing investigator-initiated trials.
      • Perform quality assurance procedures to check work of assigned staff for accuracy and completeness.
      • Work with the CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.

      Credentials and Qualifications:

      • Bachelor's degree.
        • (Science or Health care related field preferred; Masters preferred)
      • SoCRA or ACRP (or equivalent) certification.
      • Four (4) years experience in clinical trials (patient facing coordination, data management, regulatory, or other research coordination).
      • Oncology trials knowledge, OnCore CTMS experience preferred.
      • Supervisory, or team lead experience preferred

  • About the company

      H. Lee Moffitt Cancer Center & Research Institute is a nonprofit cancer treatment and research center located in Tampa, Florida.

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