242 Results for

Clinical Research Jobs in Tampa, FL

Jobs

Brandon, FL

In collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.

3 days ago

Hudson, FL

3 days ago

Tampa, FL

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.

5 days ago

Tampa, FL

Cancer Center of South Florida in partnership with Tampa General Hospital are working together to provide personalized patient care with state-of-the-art medical treatments and seeking Board Certified/Board Eligible Medical Oncologists in multiple specialties to join its team in a growing practice in Tampa, Florida. The program has a heavy focus on excellent and world class inpatient and outpatient clinical care while also being very active in Clinical Trials Research and Basic Science Translational Research.

3 days ago

Tampa, FL

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.

17 days ago

Saint Petersburg, FL

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.

30+ days ago

Brandon, FL

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.).

30+ days ago

Tampa, FL

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.

30+ days ago

Tampa, FL

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.

30+ days ago

Tampa, Florida

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.

10 days ago

Tampa, FL

$65,000–$95,000 / 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.

30+ days ago

Tampa, FL

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.

30+ 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.

30+ days ago

Tampa, FL

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.

30+ days ago

Clearwater, Florida

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;].

30+ days ago

Tampa, FL

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.

9 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.

15 days ago

Tampa, FL

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.

30+ days ago

Tampa, FL

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30+ 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.

30+ days ago

Tampa, FL

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'',''!*!

29 days ago

Clearwater, FL

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.

30+ days ago

Tampa, Florida

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.

30+ days ago

Largo, FL

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.

30+ days ago

Tampa, Florida

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.

30+ days ago

St. Petersburg, FL

$34–$35 / 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.

18 days ago

Clearwater, FL

$34–$35 / hour

15 days ago

St. Petersburg, FL

$34–$35 / hour

25 days ago

St. Petersburg, FL

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.

6 days ago

St. Petersburg, FL

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.

30+ days ago

Tampa, FL

Part time

30+ days ago

Tampa, FL

Part time

30+ days ago

Tampa, FL

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.

30+ days ago

St. Petersburg, FL

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.

30+ days ago

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

30 days ago

Tampa, FL

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

30+ days ago

Brandon, Florida

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.

13 days ago

Tampa, FL

For this reason, Moffitt has been recognized on the 2023 Forbes list of Americas Best Large Employers and Americas Best Employers for Women, Computerworld magazines list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems, and continually named one of the Tampa Bay Times Top Workplace. The EpicResearch Clinical Tools Analyst II advances Moffitts mission to prevent and cure cancer by contributing to the design, implementation, and support of clinical and enterprise applications that improve patient care, research, and operational performance.

30+ days ago

Clearwater, FL

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;].

30+ days ago

Tampa, FL

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 bachelor's degree; (c) Six years of direct experience for a master's 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.

10 days ago

Tampa, FL

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.

30+ days ago

Tampa, FL

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.

17 days ago

Riverview, FL

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.

30+ days ago

Tampa, FL

Moffitt 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.

30+ days ago

Tampa, FL

For 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.

30+ days ago

Tampa, FL

Services 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.

30+ days ago

Tampa, FL

$113,903–$142,378 / year

Leading 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.

30+ days ago

Tampa, FL

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.

18 days ago

Tampa, FL

Work 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.

30+ days ago

Tampa, FL

Associates 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.

30+ days ago

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Clinical Research Jobs in Tampa, FL

Medical Surgical Clinical Nurse Coordinator HCA Florida Brandon Hospital

Clinical Nurse Coordinator Med Surg HCA Florida Bayonet Point Hospital

Academic Benign Hematologist (Open Rank) USF Health

Medical Oncologist - Multiple Specialties Cancer Center of South Florida

Clinical Research Associate ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical and Health - Clinical Research Coord II Mindlance

Clinical Research Assistant University of South Florida

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

Clinical Research Coordinator III Care Access

Clinical Research Coordinator III Care Access Research LLC

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

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

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

Clinical Research Coordinator Alcanza Clinical Research

Clinical Trial Liaison / Clinical Research Lead ICON Plc

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

Clinical Research Nurse BayCare Health System

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

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

Pool Clinical Research Assistant Tampa General Hospital

Clinical Research Coordinator FLORIDA FERTILITY INSTITUTE PA

Clinical Research RN I CenExel

Clinical Research Assistant / Medical Assistant Alcanza Clinical Research LLC

Director of Clinical Research Site Operations CenExel

Clinical Research Nurse Coordinator Actalent Inc

Clinical Research Nurse Actalent Inc

Infusion Nurse (Clinical Research) Actalent Inc

Clinical Research Coordinator I - Oncology Johns Hopkins Hospital

Clinical Research Coordinator II - Oncology Johns Hopkins Hospital

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 Johns Hopkins Hospital

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

Clinical Manager of Research Cardiovascular Associates of America

Epic Applications Analyst II - Clinical Research Tools H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Research Coordinator Alcanza Clinical Research LLC

Research Support Specialist/Med Research Student 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

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

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

MOLECULAR GENOMICS RESEARCH SPECIALIST III H. Lee Moffitt Cancer Center & Research Institute Inc

Clinical Study Manager AxoGen Inc

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

SPVR CLINICAL TRIALS OFFICE H. Lee Moffitt Cancer Center & Research Institute Inc

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

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