ICON PlcClinical Research Associate ICON PlcClinical Research AssociateTampa, FLICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORD ASSOCIATE H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORD ASSOCIATETampa, FLOther job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors, and facilitating the collection of study-required specimens. These 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.
IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedSaint Petersburg, FLEnsure 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.
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H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR IITampa, FLCredentials and Qualifications: • Bachelor's degree with 2 years clinical trials coordination experience • In lieu of a bachelor's degree, an associate's degree with 4 years clinical trials coordination experience may be considered • CCRP/CCRC certification preferred. 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.
Care Access Research LLCClinical Research Coordinator III Care Access Research LLCClinical Research Coordinator IIITampa, FL$65,000–$95,000 / 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. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Care AccessClinical Research Coordinator III Care AccessClinical Research Coordinator IIITampa, FL$65,000–$95,000 / 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. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL 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.
University of South FloridaClinical Research Assistant University of South FloridaClinical Research AssistantTampa, FLalternative to the number of years of direct experience required, not to exceed: (a) Two years of direct experience for an associate degree; (b) Four years of direct experience for a bachelors degree; (c) Six years of direct experience for a masters degree; (d) Seven years of direct experience for a professional degree; or. USF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future.
Alcanza Clinical ResearchClinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorClearwater, FloridaScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
MindlanceClinical and Health - Clinical Research Coord II MindlanceClinical and Health - Clinical Research Coord IIBrandon, FLLogs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
Alcanza Clinical Research LLCClinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorClearwater, FLScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
H. Lee Moffitt Cancer Center & Research Institute IncSPVR RESEARCH CLINICAL MONITORING AND QUALITY TEAM H. Lee Moffitt Cancer Center & Research Institute IncSPVR RESEARCH CLINICAL MONITORING AND QUALITY TEAMFLJob Summary: The Supervisor of Research Clinical Monitoring and Quality Team supervises short-term planning, and oversight of Internal Monitoring, Quality Assurance and Clinical Research Education Training for all clinical research activities at Moffitt Cancer Center. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH BILLING SPECIALIST H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH BILLING SPECIALISTFLIn lieu of Associates degree, a High School diploma/GED plus five (5) years' experience in clinical research hospital billing/physician billing, medical audit or case management, patient financial service and/or revenue cycle billing, or clinical trails coordination is acceptable. Additionally, a Bachelors Degree plus one (1) year experience in clinical research hospital billing/physician billing, medical audit or case management, patient financial services and/or revenue cycle billing, or clinical trails coordination is acceptable.
H. Lee Moffitt Cancer Center & Research Institute IncClinical Research CTMS Calendar Build and Protocol Advisor H. Lee Moffitt Cancer Center & Research Institute IncClinical Research CTMS Calendar Build and Protocol AdvisorFLCollaboration: Foster effective collaboration with Principal Investigators, Clinical Trial Business Office staff, Clinical Trial Office personnel, Research Finance teams, monitoring teams, and Biostatisticians. By maintaining a focus on quality and collaboration, the Advisor will play an essential role in enhancing the research infrastructure and promoting best practices within the clinical trials landscape.
FLORIDA FERTILITY INSTITUTE PAClinical Research Coordinator FLORIDA FERTILITY INSTITUTE PAClinical Research CoordinatorClearwater, FLWomen's Medical Research Group i s looking for a Clinical Research Coordinator, who will play a pivotal role in advancing reproductive health research in addition to other research studies. This exciting position offers the opportunity to work closely with patients and contribute to groundbreaking studies in a supportive and innovative environment.
Johns Hopkins HospitalClinical Research Coordinator II - Oncology Johns Hopkins HospitalClinical Research Coordinator II - OncologySt. Petersburg, FLPOSITION SUMMARY: An advanced member of the study team who under the direction of the Principal Investigator and Director of Research Operations is responsible for the overall coordination of assigned studies including screening, recruitment, data collection, and data entry to ensure protocol compliance and human subjects' protection. Coordinate the preparation and submission of regulatory documentation to the sponsor and Institutional Review Board (IRB) during all phases of study conduct including start-up, continuing reviews, changes in research, problem events, and closure to ensure human subjects protections and regulatory compliance.
Johns Hopkins HospitalClinical Research Coordinator II Johns Hopkins HospitalClinical Research Coordinator IISt. Petersburg, FLSummary: An advanced member of the study team who under the direction of the Principal Investigator and Director of Research Operations is responsible for the overall coordination of assigned studies including screening, recruitment, data collection, and data entry to ensure protocol compliance and human subjects' protection. Coordinate the preparation and submission of regulatory documentation to the sponsor and Institutional Review Board (IRB) during all phases of study conduct including start-up, continuing reviews, changes in research, problem events, and closure to ensure human subjects protections and regulatory compliance.
Alcanza Clinical Research LLCClinical Research Assistant / Medical Assistant Alcanza Clinical Research LLCClinical Research Assistant / Medical AssistantLargo, FLResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH ASSOCIATE II H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH ASSOCIATE IITampa, FLMoffitt Cancer Center is a state-of-the-art NCI-designated Comprehensive Cancer Center dedicated to advancing cancer research through collaborative, team-based science. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
University of South FloridaRegional Medical Director for Child Abuse Pediatrics - Clinical Faculty Position - Assistant/Associate/Full Professor University of South FloridaRegional Medical Director for Child Abuse Pediatrics - Clinical Faculty Position - Assistant/Associate/Full ProfessorTampa, FLMuma Children's Hospital is West Central Florida's only ACS verified Pediatric Level I Trauma Center and is establishing a The Child Well‑Being Center of Excellence (COE), as a first‑in‑Florida, statewide‑recognized regional hub for pediatric trauma, child protection, and injury prevention. USF Health Child Abuse Program provides outpatient services through the community Child Advocacy Center at Mary Lees House, located in Tampa, and medical director coverage for the Children's Home Society in Polk County.
University of South FloridaChild Abuse Pediatrics Clinical Faculty Position - Assistant/Associate/Full Professor University of South FloridaChild Abuse Pediatrics Clinical Faculty Position - Assistant/Associate/Full ProfessorTampa, FLThe physician will provide comprehensive clinical services-including inpatient consultations, outpatient evaluations, forensic assessments, and multidisciplinary team collaboration - while working closely with the Department of Children and Families (DCF), child advocacy centers, law enforcement, and our hospital partner. USF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future.
National Louis University10 Month Assistant/Associate Professor of Clinical Psychology, FSPP National Louis University10 Month Assistant/Associate Professor of Clinical Psychology, FSPPTampa, FLIdeal applicants will be licensed clinical psychologists with the ability to teach doctorate-level courses in one or more of the following primary areas: Psychological Assessment (e.g., Cognitive Assessment, Objective Personality Assessment, Projective Personality Assessment, Integrative Assessment, and Psychopathology) Theory and Therapy Courses (e.g., Intervention I and II, Integrative Approaches to Psychotherapy, Child/Adolescent Therapy, Couples/Family Therapy, Child Neuropsychology) Group Psychotherapy Biological Bases and Psychopharmacology Statistics and Research Methods Bilingual (Spanish) Assessment and Intervention Social Psychology About FSPP at National Louis University The APA-Accredited Florida School of Professional Psychology PsyD program has a rich tradition of training graduates to engage the world as health-service psychologists. Essential Responsibilities In addition to teaching within their area of expertise, core faculty will: Engage in academic advising for assigned doctoral advisee Hold active membership in departmental and campus-wide governance committees Teach 24 credits per year; develop syllabi and teaching materials related to courses taught Supervise doctoral dissertations and serve on dissertation committees Participate in program assessment, student learning assessment, curriculum review, academic admissions processes, and other program activities Participate in scholarly pursuits Qualifications NLU is committed to fostering an inclusive community and strongly encourages all qualified individuals to apply.
National Louis University10-Month Assistant/Associate Professor of Clinical Psychology, FSPP National Louis University10-Month Assistant/Associate Professor of Clinical Psychology, FSPPTampa, FloridaOverview: The Florida School of Professional Psychology (FSPP) at National Louis University (NLU) located in Tampa, FL seeks exceptional practitioner-scholar applicants for Full-Time 10-Month Open Rank Professor, Clinical Psychology, a core faculty position within our APA-Accredited Clinical Psychology doctoral program. National Louis University (NLU) is looking to honor its past while defining a bold new future as a contemporary, comprehensive university that prepares diverse students for sustained professional success with a deep commitment to Access, Excellence, Innovation and Equity.
BayCare Health SystemSupervisor Research Regulatory BayCare Health SystemSupervisor Research RegulatoryTampa, FLThe supervisor directly coordinates regulatory oversight for human subjects research projects administratively approved for use within BayCare registers BayCare-sponsored projects on ClinicalTrials.gov and prepares and submits IND or IDE applications to the FDA for BayCare-sponsored projects as required. TitleSupervisor Research RegulatoryFacility BayCare System Office HybridResponsibilities IncludeResponsible for supervising a regulatory specialist team ensuring compliance with regulations managing regulations submissions to Local and Central IRBs and overseeing the preparation of necessary documentation for clinical trials.
H. Lee Moffitt Cancer Center & Research Institute IncPRN NTRO RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute IncPRN NTRO RESEARCH COORDINATOR IITampa, FLCredentials and Qualifications: Associate's degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of research or relevant experience required (may include time employed in a clinical or laboratory setting including roles such as scribe, clinical scheduling, medical assistant, laboratory or pharmacy technician); OR Bachelor's degree requires at least one (1) year of research or relevant experience; OR Master's degree no experience. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH SAMPLING COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH SAMPLING COORDINATOR IRiverview, FLAssociate's Degree in Biological Science or related field with 1 year laboratory experience in academic, industry, clinical, research, or veterinary lab (OR) Bachelor's degree in Biological Science or related field with no experience. Position Highlights: The Research Sampling Coordinator I (RSC I) assumes the responsibility of supporting and performing clinical research sample processing within the Clinical Trials Laboratory Core.
H. Lee Moffitt Cancer Center & Research Institute IncNTRO RESEARCH COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute IncNTRO RESEARCH COORDINATOR IApollo Beach, FLTeam members of NTRO work closely with community members, patients, patient families, study sponsors, and clinical teams including physicians, pharmacists, nurses, and other health care providers. Enters data and other pertinent information into the appropriate databases (i.e., Redcap, Power chart, Oncore, sponsor specific EDC system); Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.
BayCare Health SystemSupervisor Research BayCare Health SystemSupervisor ResearchTampa, FLFacilitates Research Nurse Coordinator and Principle Investigator training, oversees good clinical practice for their sites, trial quality assurance and develops any related corrective action plans. Supports the Clinical Research Manager by assisting with negotiating contracts and budgets with trial sponsors, external research agencies and investigators and prepares and assists with Administrative Review.
H. Lee Moffitt Cancer Center & Research Institute IncNTRO RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute IncNTRO RESEARCH COORDINATOR IITampa, FLAssociates degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of research or relevant experience required (may include time employed in a clinical or laboratory setting including roles such as scribe, clinical scheduling, medical assistant, laboratory or pharmacy technician); OR. Team members of NTRO work closely with community members, patients, patient families, study sponsors, and clinical teams including physicians, pharmacists, nurses, and other health care providers.
University of South FloridaResearch Support Asst University of South FloridaResearch Support AsstTampa, FLUSF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future. The ideal candidate is highly organized, demonstrates strong attention to detail, and is eager to contribute to the successful execution of clinical trials while gaining valuable experience in clinical research operations.
University of South FloridaResearch Scientist University of South FloridaResearch ScientistTampa, FLUSF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future. The positions will play a central role in running molecular, histological, behavioral, and electrochemical studies as well as maintaining laboratory efficiency, equipment maintenance, and cross-training on shared equipment.
H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH PROJECT SPECIALIST H. Lee Moffitt Cancer Center & Research Institute IncRESEARCH PROJECT SPECIALISTTampa, FLFor this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Tampa, FL Moffitt at Magnolia Campus (MCC) Clinical Science Lab Full Time - Day Shift - M-F, 8a-5p Req #: 93608 Apply Now Save Job Saved Share: At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer.
H. Lee Moffitt Cancer Center & Research Institute IncMOLECULAR GENOMICS RESEARCH SPECIALIST III H. Lee Moffitt Cancer Center & Research Institute IncMOLECULAR GENOMICS RESEARCH SPECIALIST IIITampa, FLServices supported may include: • library preparation for bulk mRNA and total RNA-seq • amplicon and capture-based whole-exome and targeted sequencing • 10X single-cell sequencing (RNA-seq, VDJ-seq, ATAC-seq, and feature barcoding) • T cell repertoire (TCR) sequencing • ATAC-seq • Microarray technologies supported include Illumina Infinium and Affymetrix arrays, and NanoString nCounter technology • Will have experience interpreting QC data from software including FASTQC, and the BaseSpace RNA-seq and DNA enrichment applications • Experience with using or implementing automation solutions on BioMek and PerkinElmer Sciclone liquid handling robotic instrumentation is a plus. These should include: • nucleic acid QC • PCR • quantitative PCR • column and bead-based nucleic acid purification • microarray processing • next-generation sequencing library preparation and QC • Experience in molecular biology with demonstrated support of a wide array of genomics technologies in the microarray and next-generation sequencing (NGS) areas, with automation experience a plus • The ability to work independently, to acquire new genomics skills rapidly, to perform multiple tasks simultaneously, and strong written and verbal communication skills are critical • In addition to bench work, experience with troubleshooting Illumina sequencing runs NGS sequencing data and instrumentation experience is required.
Johns Hopkins HospitalResearch Lab Technician Johns Hopkins HospitalResearch Lab TechnicianSt. 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. Position Summary: Under the specific direction of Shared Resources and Support, sets up and operates research instruments and applies scientific techniques and maintenance related to the Shared Resources equipment.
Catalent IncDocumentation Specialist, Analytical Research & Development Catalent IncDocumentation Specialist, Analytical Research & DevelopmentSt. Petersburg, FLInterfaces with Engineering, Procurement, Quality Control, Quality Assurance, Process Development, Project Managers, Validation and Manufacturing management in support of providing documentation support for new product introductions and for changes to existing products; Ensures that peers and supervisors are informed as to the QA issues that may arise in the projects that may affect progress. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media.
Healogics IncClinical Nurse Manager Healogics IncClinical Nurse ManagerTrinity, FL$78,900–$106,300 / yearOrganizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc. May be required to provide case management to a group of patients providing specific assessments according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.
University of South FloridaOpen Rank - MD/PhD Research University of South FloridaOpen Rank - MD/PhD ResearchTampa, FLThe department is particularly interested in candidates whose research programs will strengthen and expand existing areas of excellence in women's health, reproductive biology, maternal-fetal medicine, placental biology, gynecologic disease, reproductive endocrinology, infertility, oncology, inflammation, cardiovascular and metabolic health, and translational medicine. This position includes developing and leading an independent research program, conducting collaborative and programmatic research with departmental and institutional faculty, publishing findings in peer-reviewed journals, pursuing and securing extramural funding, and contributing meaningfully to the academic mission of the department and college.
AxoGen IncClinical Study Manager AxoGen IncClinical Study ManagerTampa, FL$113,903–$142,378 / yearLeading the development of clinical study protocols and investigational plans, case report forms and other study-specific documents (e.g., monitoring report templates, informed consent forms, monitoring plans; study guides; presentations/training materials; clinical study reports, etc.). The specific duties of the Clinical Study Manager include but are not limited to: Leading the day-to-day operations of assigned clinical studies; Serving as the study manager and primary point of contact for assigned clinical studies and managing clinical vendors such as Contract Research Organizations.
H. Lee Moffitt Cancer Center & Research Institute IncSPVR CLINICAL TRIALS OFFICE H. Lee Moffitt Cancer Center & Research Institute IncSPVR CLINICAL TRIALS OFFICETampa, FLWork with the CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions. Position Highlights: • Provides basic day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible CTO manager and in collaboration with faculty and investigators.
Florida Cancer Specialists and Research InstituteClinical Medical Physicist I Florida Cancer Specialists and Research InstituteClinical Medical Physicist IHudson, FLThis includes consultation with physicians, as well as treatment plan development and implementation in collaboration with members of the radiation oncology team (i.e. physicians, dosimetrists, therapists, and nursing staff), and quality assurance of treatment delivery and systems. Supports all on-site Continuous Quality Improvement (CQI) initiatives including but not limited to - daily team huddle, weekly chart rounds, monthly technical reviews, CQI committees and sub-committees.
Banfield Pet HospitalClinical Studies Accounting Support - Mars Veterinary Health Banfield Pet HospitalClinical Studies Accounting Support - Mars Veterinary HealthTampa, FL$29.04–$45.37 / hourThe CSAS works with study sponsors the MVH Clinical Studies team, and MVH clinical study sites to support and provide guidance on the administration of the financial, compliance, personnel, and other related aspects of the clinical studies. Assists in development of materials and tools necessary to appropriately train individuals involved in the conduct of the studies and establishes and organizes study files, including but not limited to, study and/or regulatory binders, study specific source documentation, and other materials.
Elevance Health IncClinical Provider Auditor II - Payment Integrity SIU Elevance Health IncClinical Provider Auditor II - Payment Integrity SIUTampa, FLMinimum Requirements: Requires a AA/AS and minimum of 3 years medical coding/auditing experience, including minimum of 1 year in fraud, waste abuse experience; or any combination of education and experience, which would provide an equivalent background. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
H. Lee Moffitt Cancer Center & Research Institute IncEPIC BEAKER CLINICAL APPLICATIONS ANALYST III - $10K Sign-On Bonus H. Lee Moffitt Cancer Center & Research Institute IncEPIC BEAKER CLINICAL APPLICATIONS ANALYST III - $10K Sign-On BonusFLThe Epic Beaker Clinical Applications Analyst Ill plays a vital role in advancing Moffitt's mission to prevent and cure cancer by leading the design, implementation, and optimization of clinical and enterprise applications that directly support patient care, research, and operational excellence. Remote applicants from the following states are encouraged to apply: Alabama, Arizona, Arkansas, Florida, Georgia, Idaho, Indiana, Iowa, Kansas, Louisiana, Mississippi, Missouri, Montana, North Carolina, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, or Wyoming.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL TRIALS SCREENING COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL TRIALS SCREENING COORDINATOR ITampa, FLn \nSuccessful candidates will possess: \n\n Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills \n Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences \n Prior experience in clinical trials is preferred \n Familiarity with regulatory requirements in clinical research or ability to successfully learn this \n Experience interacting with patients and coordinating care with medical staff \n Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol\n \nJob Summary\n \nThe Clinical Trials Screening Coordinator I reports to the Clinical Trials Office but will directly support a specific Disease Site Program. \n \nhttps://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ \n \nClinical Trials \n \nThese 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.
University of South FloridaPostdoctoral Scholar Clinical University of South FloridaPostdoctoral Scholar ClinicalTampa, FLUSF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future. DUTIES: TEACHING 2% Fellowship includes presentation/teaching though any of the following: grand rounds, teaching rounds, journal club, didactic series, university or community lectures, assisting faculty with preparation of teaching materials.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RSCH REV CYCLE QUALITY AUDITOR I H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RSCH REV CYCLE QUALITY AUDITOR IFLThe Clinical Research Revenue Cycle (CRRC) Quality Auditor I is responsible for executing and documenting data and quality audits within Moffitt CRRC teams for purposes of examining associated risks and evaluating the effectiveness of the CRC control environment, including monitoring adherence to established policies, external agency regulations, and industry best practices implemented. Responsibilities: With Supervisor support, meet with subject matter experts to understand scope of audit, identify risks and mitigating controls, define the population to audit, and work with process owners to obtain the necessary documents.
Florida Cancer Specialists and Research InstituteClinical Oncology Pharmacist (Hybrid) Florida Cancer Specialists and Research InstituteClinical Oncology Pharmacist (Hybrid)Tampa, FLUnder the direction of the Associate Director of Pharmacy Clinical Services, the Clinical Oncology Pharmacist works collaboratively with Hematology/Oncology physicians and nursing staff to provide quality patient care appropriate for the patient's oncologic diagnosis, prescribed treatment, age group and other identified needs. The pharmacist coordinates the drug therapy process on Hematology/Oncology patient population which may include any of the following activities but is not limited to drug selection (including the use of genetic/biomarker testing in the drug selection process), drug information, dosing, monitoring, outcomes management, retrospective drug utilization monitoring and compliance.
Compass Group North AmericaCLINICAL DIETITIAN Compass Group North AmericaCLINICAL DIETITIANTampa, FL$70,000–$85,000 / yearOur company has earned significant recognition, including being named one of Modern Healthcares Top 100 Best Places to Work in Healthcare for five consecutive years and appearing on Training Magazines Top 125 Organizations list for six straight years. Compass Group employs over 3000 RDNs across the United States, making us one of the nations largest employers of Dietitians in a variety of settings.
Medtronic PlcClinical Specialist Opportunities for National Sales Network Career Event - Aug. 12-14, Washington DC Medtronic PlcClinical Specialist Opportunities for National Sales Network Career Event - Aug. 12-14, Washington DCTampa, FLThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). Peripheral & Endovenous: Peripheral and Superficial Venous Interventions (SVI) therapies are a critical part of the Medtronic vascular portfolio, treating patients with a broad range of conditions, including Peripheral and Carotid Disease, End Stage Renal Disease, Peripheral Embolization, and Superficial and Deep Venous Disease.