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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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Dr. Giuliano leads multiple domestic and multinational studies, including development of early detection cancer biomarkers, clinical trials for the prevention of HPV-related cancers among people living with HIV in Latin America and the Caribbean, and research of understudied virally-associated cancers among men and women living with HIV in sub-Saharan Africa.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States.
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Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols.
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As the hub for all cancer research activities, this office supports all aspects of research including but not limited to trial feasibility, activation, recruitment, and enrollment into Phase I-IV clinical trials; enhancing the opportunities for treatment options for patients in the Tampa Bay area.
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Incorporate strategies and education to improve patient screening and enrollment onto Moffitt clinical trials. Support patients interested in clinical trials via email and phone line, connecting them with appropriate Moffitt and community resources.
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Lead biomarker and pharmacokinetic planning, definition, and implementation, overseeing sample collection for early and late-phase clinical trials. Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development.
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Excellent independent writing and verbal communication skills a mustThorough understanding of local and international regulations applicable to clinical development· Track record of excellence in designing, defending, and executing clinical development plans and clinical studiesDemonstrated expertise in managing clinical programs, either pre- or post-approval; expertise in managing large clinical programs (or adaptive clinical trials seeking conditional approval) preferred.
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The Foundation for Sickle Cell Disease Research (FSCDR) is the United States’ first outpatient center exclusively dedicated to the acute treatment of and innovative research for SCD. Florida has the highest population of individuals living with SCD in the U.S. In 2012, we opened our first center in Hollywood, FL, offering focused care and collecting data through clinical trials.
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Provides troubleshooting and other technical assistance to clinical trials personnel and CVRx employees. The Account Manager will provide market development expertise, technical case support, educational support and patient recruitment support to trial sites participating in CVRx clinical research and commercial sites.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Conduct cognitive, diagnostic, and clinical assessments of study participants, as well as caregiver interviews for clinical trials under the direction of a supervising Principal Investigator in accordance to FDA, GCP, and protocol guidelines.
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clinical trials jobs in Brandon, FL
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