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MC
Moffitt Cancer Center
MGR CLINICAL TRIALS OFFICE
Career Insights for Clinical Trial Manager
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What they do
A Clinical Trial Manager is responsible for planning and managing all aspects of an organization's program of clinical trials, usually for an organization undertaking pharmacological drug testing.
$116,988 / year median in Florida
Job Description
MGR CLINICAL TRIALS OFFICE 3.9 3.9
out of 5 stars 16380 Wilton Way, Land O' Lakes, FL 34638 Full-time Moffitt Cancer Center 782 reviews Full-time 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 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times' Top Workplaces. Summary This position will be on site/remote This will be for our Hematology/Myeloid team.Position Highlights:
- Responsible for the direct supervision of clinical research staff
- Leads the daily clinical research operations for one or more key areas
- Responsible for monitoring workloads and determining appropriate staffing levels for the clinical research staff (nurses, coordinators, and data specialists)
- Takes the lead and/or participates in development and execution of training/mentoring programs, quality improvement processes and other projects, including the development of SOP's
- Works in collaboration with the Clinical Trials Business Office and Research Finance to coordinate budget development and research patient and sponsor billing
- Responsible for budgeting and financial management of one or more cost centers
Responsibilities:
- Staff supervision and mentoring, monitor staff conduct, perform staff interviews, recommend hire/terminations, and perform annual staff evaluations
- Allocates staff based on patient acuity, staffing standards and expertise of personnel
- Fiscal oversight-develop annual budget for the Clinical Trials Office cost center, review individual protocol budgets to assure adequate data management reimbursement; responsible for revenue creation, cost management and purchasing
- Actively participate in operational review of new protocols and amendments for feasibility of conduct
- Assist with development, revision and continuous evaluation of clinical research department standards and policies; participate in and/or lead process improvement working groups and staff mentoring education activities
Credentials and Qualifications:
- Bachelor's degree (Master's preferred)
- Five (5) years of experience in executing multidisciplinary clinical research protocols (preferably in oncology)
- Two (2) years of staff supervisory/management experience
- Clinical Research Certification (e.