Find & Apply For Clinical Research Manager Jobs In Hillsborough, Florida
Clinical Research Manager jobs in Hillsborough, Florida involve overseeing research projects, managing staff, and ensuring compliance with regulations. Responsibilities include developing protocols, monitoring data collection, and analyzing results. Strong leadership and organizational skills are essential for this role. Below you can find different Clinical Research Manager positions in Hillsborough, Florida.
Jobs in Hillsborough
Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.
SPVR CLINICAL TRIALS OFFICE
H. Lee Moffitt Cancer Center & Research Institute
Hillsborough, FL
Manager Clinical Research – Cardiology and Internal Medicine
BayCare
Hillsborough, FL
Clinical Research Supervisor (Oncology)
Actalent
Hillsborough, FL
Latest Jobs in Hillsborough
Salary Information & Job Trends In this Region
Clinical Research Managers in Hillsborough, Florida oversee clinical trials and ensure compliance with regulatory standards. - Entry-level Clinical Research Coordinator salaries range from $45,000 to $55,000 per year - Mid-career Clinical Research Manager salaries range from $65,000 to $80,000 per year - Senior Clinical Research Director salaries range from $90,000 to $120,000 per year The role of a Clinical Research Manager in Hillsborough has a substantial history, closely linked with the development of medical facilities and research institutions in the area. These professionals have played a pivotal role in advancing medical research and patient care standards. Over the years, the responsibilities and scope of Clinical Research Managers in Hillsborough have expanded significantly. This evolution is largely due to advances in clinical research methodologies, regulatory complexities, and the increasing importance of clinical trials in medical advancements. Current trends in the field include a greater emphasis on digital data management, patient-centric trial designs, and adaptive trial protocols that allow for more flexibility in response to emerging data. This shift is aligned with global trends towards more efficient and ethical research practices.
