86 Results for

Clinical Research Coordinator 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.

5 days ago

Hudson, FL

5 days ago

Hudson, FL

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. As a majority owner of Galen College of Nursing, which joins Research College of Nursing and Mercy School of Nursing as educational facilities within the HCA Healthcare family, we make it easier and more affordable to gain certifications and job skills.

5 days ago

St Petersburg, FL

5 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

Tampa, FL

$65,000–$95,000 / year

15 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

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.

8 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

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

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

St. Petersburg, FL

1 day 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

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.

20 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

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, 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

Brandon, FL

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.

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

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.

1 day 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

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.

20 days ago

Tampa, FL

n \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.

30+ days ago

Tampa, FL

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. 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.

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

Clearwater, FL

$34–$35 / hour

17 days ago

St. Petersburg, FL

$34–$35 / hour

27 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

Brandon, FL

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.

13 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.

19 days ago

Brandon, FL

7 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

Tampa, FL

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30+ days ago

New Port Richey, FL

Location: Morton Plant North Bay Hospital Facility: BayCare Health System Laboratory Services - NBH Shift: Nights | 9:00 PM - 7:00 AM Schedule: Full-Time | Onsite Weekend Work: Every Other Weekend. Supported by more than 30,000 team members, BayCare promotes a forward‑thinking philosophy built on trust, dignity, respect, responsibility, and clinical excellence.

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

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

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

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.

19 days ago

Tampa, FL

Tissue Core is staffed by a multidisciplinary team of over 40 professionals, including Biorepository Coordinators, Research Specialists, Staff Scientists, Supervisors, Team Leads, Research Pathologists, and Administrators. Established in 1992, our mission is to collect, process, store, and distribute high-quality, annotated biospecimens to support innovative oncology research across basic, population, clinical, and translational disciplines.

19 days ago

Tampa, FL

Under supervision of the Director of Bone Marrow Transplant (BMT) and Cellular Therapy Program, the ONC Transplant Coordinator coordinates evaluation and preparation of patients for Hematopoietic Stem Cell (HSC) transplantation, cellular therapies and long-term management of patients post-treatment. ''679171'',''true'',''679171'',''false'',''Submission for the position: Oncology Transplant Coordinator - Bone Marrow Transplant Cell Therapy - (Job Number: 260001U2)'',''false'',''679171'',''false'',''true'',''Oncology Transplant Coordinator - Bone Marrow Transplant Cell Therapy'',''260001U2'',''!*!

30+ days ago

Tampa, FL

Muma 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.

30+ days ago

Tampa, FL

The Counseling Center, with a dedicated, energetic, and motivated team of 30 multidisciplinary professionals including licensed psychologists, licensed mental health counselors, licensed clinical social workers, licensed marriage and family therapists, and administrative support personnel is accredited by IACS and has an APA-accredited doctoral internship and APPIC affiliated post-doctoral fellowships. 10%: Supervises the clinical, academic, and research experiences of post-doctoral fellows, doctoral level clinical and counseling psychology interns, and practicum students enrolled in mental health academic training programs (e.g., clinical psychology, counseling psychology, social work, mental health counseling, school psychology).

12 days ago

Tampa, FL

The Advanced Lung Disease (ALD) Coordinator is responsible for collaborating with the healthcare team to develop theory-based patient care for patients undergoing advanced or end-stage organ disease, from referral through long-term follow-up care. ''678954'',''true'',''678954'',''false'',''Submission for the position: Advanced Lung Disease Coordinator - Transplant Lung Program - (Job Number: 260001SY)'',''false'',''678954'',''false'',''true'',''Advanced Lung Disease Coordinator - Transplant Lung Program'',''260001SY'',''!*!

30+ days ago

St. Petersburg, FL

Working closely with the Study Start Up Manager, Clinical Research Managers and study teams, this person will coordinate the submission of initial Institutional Review Board (IRB) applications for complex clinical research studies. 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.

19 days ago

Trinity, FL

$78,900–$106,300 / year

Organizes 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.

30+ days ago

Trinity, Florida

Job Summary: The purpose of the Wound Care Nurse position is to support the nursing department and facility wide directives through specialized focus on Wound Care Specialist (WCS) This job description is not an all- inclusive list of essential functions for the job described, but rather a general description of some of the responsibilities necessary to carry out the duties of this position. Supports the facility and medical staff, departments and teams including guidance, training, technical support, celebrating successes and continued learning related to infection prevention.

14 days ago

Trinity, Florida

14 days ago

St. Petersburg, FL

As the only pediatric affiliate of Moffitt Cancer Center and a FACT-accredited program, patients also benefit from access to leading-edge research, clinical trials, and advanced stem cell therapies - all while receiving compassionate, family-centered care in a dedicated pediatric transplant unit. 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.

30+ days ago

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Clinical Research Coordinator Jobs in Tampa, FL

Medical Surgical Clinical Nurse Coordinator HCA Florida Brandon Hospital

Clinical Nurse Coordinator Med Surg HCA Florida Bayonet Point Hospital

RN Charge Clin Coordinator Cardiac PCU HCA Florida Bayonet Point Hospital

Charge Nurse Acute Care HCA Florida Northside Hospital

Clinical Research Coordinator III Care Access Research LLC

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

Clinical Research Coordinator III Care Access

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

Clinical Research Coordinator I - Oncology Johns Hopkins Hospital

Clinical Research Coordinator Alcanza Clinical Research

Clinical Research Coordinator FLORIDA FERTILITY INSTITUTE PA

Clinical Research Coordinator II - Oncology Johns Hopkins Hospital

Clinical Research Coordinator II Johns Hopkins Hospital

Clinical Research Coordinator Johns Hopkins Hospital

Clinical Research Nurse Coordinator Actalent Inc

Clinical Research Coordinator Alcanza Clinical Research LLC

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

Clinical Research Assistant University of South Florida

Research Coordinator Cardiovascular Associates of America

Clinical and Health - Clinical Research Coord II Mindlance

Research Clinical Assistant Florida Cancer Specialists and Research Institute

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

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

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

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

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

Clinical Research Nurse Actalent Inc

Infusion Nurse (Clinical Research) Actalent Inc

Clinical Research Assistant / Medical Assistant Alcanza Clinical Research LLC

Clinical Manager of Research Cardiovascular Associates of America

Clinical Research Associate ICON Plc

Medical Surgical Clinical Nurse Coordinator HCA Healthcare

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Pool Clinical Research Assistant Tampa General Hospital

Clinical Laboratory Scientist Coordinator BayCare Health System

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

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

Clinical Research Nurse BayCare Health System

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

Supervisor Research BayCare Health System

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

Oncology Transplant Coordinator - Bone Marrow Transplant Cell Therapy Tampa General Hospital

Regional Medical Director for Child Abuse Pediatrics - Clinical Faculty Position - Assistant/Associate/Full Professor University of South Florida

Clinical Psychologist University of South Florida

Advanced Lung Disease Coordinator - Transplant Lung Program Tampa General Hospital

Regulatory Coordinator I - Study Activation Johns Hopkins Hospital

Clinical Nurse Manager Healogics Inc

Wound Care Coordinator (RN) Trinity Regional Rehab Center

Wound Care Coordinator (LPN) Trinity Regional Rehab Center

RN Clinical Database Administrator - BMT Johns Hopkins Hospital

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