165 Results for

Research Jobs in Gibsonton, FL

Jobs

Tampa, FL7 days ago

The role includes a 2/8ths appointment at the VA, focused on clinical care for malignant hematology cases (Hodgkin’s and non-Hodgkin’s lymphoma) with and without fellows present, taking 3 weekend calls per year, and supervision of fellows managing chemotherapy-unit clinical issues. The Morsani College of Medicine, Department of Internal Medicine, Division of Hematology, is seeking an Academic Hematologist (Open Rank) with a strong interest in benign/classical hematology.

Tampa, FL30+ days ago

TGH Main Campus'',''1 Tampa General Circle'','' '',''Tampa'',''33601'',''On Site'',''On Site'',''Clinical Research'',''Clinical Research'',''Florida Health Sciences Center Tampa General Hospital'',''Florida Health Sciences Center Tampa General Hospital'',''Per Diem/Pool'',''Per Diem/Pool'','''','''',''Night Job'',''Night Job'','''','''',''On Site'',''On Site'','''','''','''','''',''Varies'',''Varies'',''22.32'',''22.32'',''May 21, 2026, 3:50:22 PM'',''May 21, 2026, 3:50:22 PM'',''false'',''679361'',''679361'',''true'',''679361'',''false'',''Submission for the position: Pool Clinical Research Assistant - (Job Number: 260001WV)'',''false'',''679361'',''false'',''true''. ''679361'',''true'',''679361'',''false'',''Submission for the position: Pool Clinical Research Assistant - (Job Number: 260001WV)'',''false'',''679361'',''false'',''true'',''Pool Clinical Research Assistant'',''260001WV'',''!*!

Tampa, FL30+ days ago

alternative 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.

Lakeland, FL26 days ago

Responsibilities 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.

Largo, FL30+ days ago

Lakeland, Florida27 days ago

Responsibilities 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.

New!

St. Petersburg, FL1 day ago

POSITION 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.

Tampa, FL30+ days ago

$65,000–$95,000 Per Year

With 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.

St. Petersburg, FL30+ days ago

Tampa, Florida12 days ago

With 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.

St. Petersburg, FL30+ days ago

POSITION SUMMARY: The Clinical Research Coordinator is a 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 minimal-risk studies, including regulatory submissions, 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' protection and regulatory compliance.

New!

Tampa, FL1 day ago

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. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption.

Clearwater, Florida30+ days ago

Scheduling 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;].

Brandon, FL30+ days ago

You’ll be working on site at 635 Eichenfeld Drive, Brandon, FL 33511, where you will lead the growing program of cardiovascular medicine research, with opportunities to collaborate with teams nationwide. About CVAUSA: Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes.

St. Petersburg, FL20 days ago

$34–$35 Per Hour

You will work with consented patients enrolled in clinical trials, providing high-quality patient care and infusion services while supporting study-related procedures and documentation. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clearwater, FL17 days ago

$34–$35 Per Hour

St. Petersburg, FL27 days ago

$34–$35 Per Hour

Tampa, FL19 days ago

ICON 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.

Saint Petersburg, FL30+ days ago

Ensure 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.

Tampa, FL30+ days ago

Credentials 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.

Tampa, Florida30+ days ago

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.

Clearwater, FL30+ days ago

Women'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.

Tampa, Florida30+ days ago

Please be sure to attach all required documents listed below in the attachment box at the bottom of the "My Experience" page of the application before continuing through the application. To receive full consideration for employment with The University of Tampa, please be sure to submit/upload required documents for this position at time of application submission.

Tampa, Florida30+ days ago

Develops budget and ensures financial and operational metrics are meeting organizational objectives by identifying, analyzing, and monitoring issues that affect profitability, growth, and productivity. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.

FL30+ days ago

In 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.

Tampa, FL30+ days ago

Other 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.

Bradenton, FL27 days ago

May be responsible for providing coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III. Candidates must have a valid RN license, in state of employment, a minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience.

Tampa, FL30+ days ago

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. 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.

Tampa, FL30+ days ago

Part-time

Tampa, FL30+ days ago

Part-time

Tampa, FL30+ days ago

The Clinical Research RN I (CRN I) facilitate clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol\u2010related care of patients enrolled in clinical trials. In addition, this position is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking.

St. Petersburg, FL8 days ago

Under the direction of the Principal Investigator and research leadership, the CRC I is responsible for coordinating assigned clinical studies, including participant recruitment, regulatory submissions, data collection, and study documentation to ensure protocol compliance and protection of human subjects. We 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.

Bradenton, FL30+ days ago

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. 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.

FL17 days ago

Job 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.

Brandon, FL30+ days ago

Logs/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.).

Tampa, FL30+ days ago

Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers, and thousands of physicians. Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion.

Tampa, FL11 days ago

Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc. Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer.

Tampa, FL20 days ago

Credentials 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.

Brandon, FL13 days ago

Full-time

This role serves as the primary on-site leader of the research team, partnering closely with physicians, clinical staff, and national research leadership to build and manage a high-performing research program that advances innovation in cardiovascular medicine. This role requires a proactive leader who can champion research within the practice, mentor staff, implement scalable processes, and advocate for research growth among physician partners and operational leadership.

St. Petersburg, FLORIDA30+ days ago

Remote

You will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.

FL30+ days ago

Collaboration: 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.

FL30+ days ago

SUPERVISOR CLINICAL RESEARCH OPERATIONS PRE AWARD - H. Lee Moffitt Cancer Center & Research Institute Inc.

Tampa, FL30+ days ago

Lee Moffitt Cancer Center & Research Institute Inc. CLINICAL RESEARCH EDUCATION SPECIALIST - H.

Tampa, FL30+ days ago

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. conducting tests,sample inventory, basic cell culture tasks, RNA extraction, DNA extraction, qPCR, ELISA, staining and imaging cells.

Tampa, FL12 days ago

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. Through these programs, we prepare students to succeed in an increasingly diverse world that demands skills in communication, leadership, problem solving, critical and analytical reasoning, methodological thinking, statistical analysis, and multicultural and global understanding.

Tampa, FL30+ days ago

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. 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.

Tampa, FL19 days ago

Facilitates 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.

Riverview, FL30+ days ago

Associate'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.

Tampa, FL30+ days ago

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Tampa, FL15 days ago

Our core value of Commitment is paramount as you will assist in providing business process narratives and flowcharts to provide a description of how personnel perform a specific business process, the risks the process poses, and the controls required to mitigate those risks. Government Finance and Execution including use of systems such as: Wide Area Workflow (WAWF), EDA, DEAMS, GFEBS, NERP, SABRS, CRISA, DAI, ADVANA, TS/SCI Clearance.

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Research Jobs in Gibsonton, FL

Academic Benign Hematologist (Open Rank) USF Health

Pool Clinical Research Assistant Tampa General Hospital

Clinical Research Assistant University of South Florida

Clinical Research Assistant Alcanza Clinical Research LLC

Clinical Research Assistant / Medical Assistant Alcanza Clinical Research LLC

Clinical Research Assistant/ Medical Assistant Alcanza Clinical Research

Clinical Research Coordinator II Johns Hopkins Hospital

Clinical Research Coordinator III Care Access Research LLC

Clinical Research Coordinator II - Oncology Johns Hopkins Hospital

Clinical Research Coordinator III Care Access

Clinical Research Coordinator Johns Hopkins Hospital

Research Clinical Assistant Florida Cancer Specialists and Research Institute

Clinical Research Coordinator Alcanza Clinical Research

Research Coordinator Cardiovascular Associates of America

Clinical Research Nurse Coordinator Actalent Inc

Clinical Research Nurse Actalent Inc

Infusion Nurse (Clinical Research) Actalent Inc

Clinical Research Associate ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

CLINICAL RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Research RN I CenExel

Clinical Research Coordinator FLORIDA FERTILITY INSTITUTE PA

Part-time Temporary Research Assistant University of Tampa

Director of Clinical Research Site Operations CenExel

CLINICAL RESEARCH BILLING SPECIALIST H. Lee Moffitt Cancer Center & Research Institute Inc

CLINICAL RESEARCH COORD ASSOCIATE H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Research Coordinator III Drug Development Unit Florida Cancer Specialists and Research Institute

CLINICAL RESEARCH COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Research RN I ForCare Clinical Research

Director of Clinical Research Site Operations ForCare Clinical Research

CLINICAL RESEARCH RN I H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Research Coordinator I - Oncology Johns Hopkins Hospital

Research Pharmacy Coordinator I Florida Cancer Specialists and Research Institute

SPVR RESEARCH CLINICAL MONITORING AND QUALITY TEAM H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical and Health - Clinical Research Coord II Mindlance

Clinical Research Nurse BayCare Health System

Clinical Trial Liaison / Clinical Research Lead ICON Plc

PRN NTRO RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Manager of Research Cardiovascular Associates of America

Remote Market Research Assistant Earn Up to $50/Task Occupons Quebec

Clinical Research CTMS Calendar Build and Protocol Advisor H. Lee Moffitt Cancer Center & Research Institute Inc

SUPERVISOR CLINICAL RESEARCH OPERATIONS PRE AWARD H. Lee Moffitt Cancer Center & Research Institute Inc

CLINICAL RESEARCH EDUCATION SPECIALIST H. Lee Moffitt Cancer Center & Research Institute Inc

Research Assistant University of South Florida

OPS Social Science Research Assistant University of South Florida

Research Support Asst University of South Florida

Supervisor Research BayCare Health System

RESEARCH SAMPLING COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute Inc

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

FIAR Consultant-Research Assistant (Top Secret Clearance Required) St. Michael's Inc

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