NewBilingual Registered Dietitian Clinical Research - PRN Professional Case ManagementBilingual Registered Dietitian Clinical Research - PRNTampa, FLPerforms the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
Registered Nurse (RN) - Inpatient Clinical Informatics - $35 per hour Tampa General HospitalRegistered Nurse (RN) - Inpatient Clinical Informatics - $35 per hourTampa, FLConsistently recognized for world-class care, Tampa General Hospital is ranked as the #1 hospital in Tampa Bay by U.S. News & World Report for 2025-26 and is nationally ranked among the top 50 hospitals in the nation in six specialties. Collaborates with Pediatric Trauma Medical Director, Pediatric Trauma APRN and Pediatric Trauma Program Coordinator to provide clinical and systems oversight and trauma education to ensure provision of efficient, quality care.
Clinical Research Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedTampa, FL$71,900–$189,000 / yearIn this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.
Clinical Research Assistant - Core-Ctr For Research Excel The Tampa General Hospital Foundation IncClinical Research Assistant - Core-Ctr For Research ExcelTampa, FLKey duties include pre-screening potential participants against protocol eligibility criteria; obtaining and documenting informed consent for non-interventional registry/observational studies and select minimal-risk device studies; assisting with subject enrollment, randomization, and coordination of research visits; reviewing study lab manuals and collecting/processing specimens per protocol; performing accurate data entry from source documents to paper/electronic case report forms (including redaction as requested); and serving as a liaison between research staff and departments where research is conducted, along with other assigned tasks. The Clinical Research Assistant supports multiple clinical research projects under the supervision of the Clinical Research Supervisors and Clinical Research Managers.
NewClinical Research Associate II IREClinical Research Associate IITampa, FloridaWilling and able to travel up to 60% - 75% for on-site monitoring visits across southeast region; preference given to candidates residing in Tampa near major HUB airports to support efficient regional travel. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
Clinical Research Assistant - Core-Ctr For Research Excel Tampa General HospitalClinical Research Assistant - Core-Ctr For Research ExcelTampa, FL''684173'',''true'',''684173'',''false'',''Submission for the position: Clinical Research Assistant - Core-Ctr For Research Excel - (Job Number: 260003F0)'',''false'',''684173'',''false'',''true'',''Clinical Research Assistant - Core-Ctr For Research Excel'',''260003F0'',''!*! The Clinical Research Assistant supports multiple...
Clinical Research Coordinator(Onsite) Nesco Resource, LLCClinical Research Coordinator(Onsite)Brandon, FLThe Research Coordinator is responsible for coordinating multiple clinical research protocols and serving as a liaison between investigators, sponsors, and internal stakeholders. Participate in investigator meetings, sponsor calls, and internal CRC meetings.
NewClinical Research Associate II ICON PlcClinical Research Associate IITampa, FLWilling and able to travel up to 60% - 75% for on-site monitoring visits across southeast region; preference given to candidates residing in Tampa near major HUB airports to support efficient regional travel. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
NewClinical Research Coordinator BayCare Health SystemClinical Research CoordinatorTampa, FLRequired - 5 years research experience with an Associates degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory). Or - 2 years of research experience with an Associates Degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory).
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedSaint Petersburg, FL$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Coordinator II Care AccessClinical Research Coordinator IISt. Petersburg, Florida$60,000–$90,000 / yearWith programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
Clinical Research Assistant (Tuesday - Saturday) Care AccessClinical Research Assistant (Tuesday - Saturday)Brandon, Florida$19–$33 / hourAbility and willingness to work independently with minimal supervision Ability to learn to work in a fast-paced environment Excellent communication skills and a high degree of professionalism with all types of people Excellent organizational skills with strong attention to detail A working knowledge of medical and research terminology A working knowledge of federal regulations, Good Clinical Practices (GCP) Critical thinker and problem solver Friendly, outgoing personality with the ability to maintain a positive attitude under pressure Contribute to team and site goals Proficiency in Microsoft Office Suite High level of self-motivation and energy An optimistic, “can do” attitude Certifications/Licenses, Education, and Experience . Request study participant payments Schedule visits with participants, contact with reminders Request medical records of potential and current research participants Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc., under the direction of the CRC Ability to understand and follow institutional SOPs Documentation Record data legibly and enter in real time on paper or e-source documents Update all applicable internal trackers and online recruitment systems Assist with recruitment of new participants by conducting phone screenings Patient Recruitment Assist with preparation of outreach materials .
CLINICAL RESEARCH COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR ITampa, FLThese positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities.
Clinical Research Nurse BayCare Health SystemClinical Research NurseSt Petersburg, FLOur network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. Creation and completion of source worksheets, Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion.
NewClinical Research Data Coordinator 1 - PM Biorepository Tampa General HospitalClinical Research Data Coordinator 1 - PM BiorepositoryTampa, FLWhile the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the data coordinator plays a critical role in the study by reviewing, extracting, cleaning, and auditing data from various source documents so that the appropriate data can be shared. ''685288'',''true'',''685288'',''false'',''Submission for the position: Clinical Research Data Coordinator 1 - PM Biorepository - (Job Number: 260003TN)'',''false'',''685288'',''false'',''true'',''Clinical Research Data Coordinator 1 - PM Biorepository'',''260003TN'',''!*!
NewClinical Research Assistant Florida Cancer Specialists and Research InstituteClinical Research AssistantSt. Petersburg, FLWe 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. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption.
Clinical Research Assistant Tuesday - Saturday Care Access Research LLCClinical Research Assistant Tuesday - SaturdayBrandon, FL$19–$33 / hourWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Assistant (Tuesday - Saturday) is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.
NewClinical Research Data Coordinator 1 - PM Biorepository The Tampa General Hospital Foundation IncClinical Research Data Coordinator 1 - PM BiorepositoryTampa, FLWhile the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the data coordinator plays a critical role in the study by reviewing, extracting, cleaning, and auditing data from various source documents so that the appropriate data can be shared. Intermediate knowledge of spreadsheets (such as Excel), familiarity with databases (ex: RedCAP, iMedra, Medidata, Velos, etc.) and ability to work with large volumes of data with a high degree of accuracy.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIATampa, FLDeprecated : preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85 .
Clinical Research Coordinator II Johns Hopkins HospitalClinical Research Coordinator IISt. Petersburg, FLWe are committed to creating a welcoming and inclusive environment, where we embrace and celebrate our differences, where all employees feel valued, contribute to our mission of serving the community, and engage in equitable healthcare delivery and workforce practices. This role is responsible for coordinating complex clinical studies, ensuring regulatory compliance, supporting patient enrollment and follow-up, and collaborating with investigators, research staff, sponsors, and study participants.