CLINICAL TRIAL ACTIVATOR

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. 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. Join a dedicated team of nearly 10,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time's Top Workplaces. A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001.

Summary Job Summary:

The Clinical Trials Activator is responsible for managing the startup of new clinical trials, ensuring adherence to institutional policies, activation timelines and key performance metrics. Through influence leadership, effective communication, and independent decision making, this role leads the study activation process, ensuring teams adhere to completion timelines, tracking and reporting regular progress updates on activation tasks and milestones, and collaborating with key internal and external stakeholders to efficiently prepare and operationalize new clinical trials. This position drives outstanding cooperation, collaboration and accountability among investigators, research teams, collaborating departments, and external study sponsors to ensure an optimized and cohesive study startup process. This role effectively problem solves and overcomes barriers to timely, accurate activation as they occur, escalating to senior leadership as necessary. This position is also responsible for ensuring thorough, accurate, compliant preparation of essential research materials and documentation and the readiness of all who will be involved in the conduct of study.

Minimum Experience Required:

Bachelor's degree with three (3) years of experience in clinical trials (patient facing coordination, data management, regulatory, activation, or other relevant clinical research experience). In lieu of bachelor's degree: • an associate's degree and five (5) years' experience in clinical trials (patient facing coordination, data management, regulatory, or other relevant clinical research experience), OR • a high school diploma and seven (7) years' experience in clinical trials (patient facing coordination, data management, regulatory, or other relevant clinical research experience).

Certification Required:

Clinical Research Certification CCRP from SOCRA, Clinical Research Certification CCRC from

ACRP, OR

Certified associate in project management (CAPM) will also be accepted. •Can obtain certification of choice within one (1) year of starting in position•