Spvr Clinical Trials Office

3 weeks ago

Tampa, United States Moffitt Cancer Center Full time

At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.

Summary

The Clinical Trials Office-Heme/Myeloma Data Management Department is looking for a Clinical Trials Supervisor.

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

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