Clinical Research Nurse / Paramedic, Early Phase Clinical Trials - Daytona Beach, FL Fortrea IncClinical Research Nurse / Paramedic, Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FLClear Shift Structure: Work primarily 10‑hour shifts during the week, with extended 12‑hour coverage on weekends as needed-providing consistency while supporting critical study operations. We are seeking a dedicated rotating shift Clinical Research Nurse / Paramedic to support the execution of innovative Early Phase clinical trials, ensuring participant safety and protocol accuracy.
NewClinical Research Registered Nurse, Early Phase Clinical Trials - Daytona Beach, FL Fortrea IncClinical Research Registered Nurse, Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FLClear Shift Structure: Work primarily 10‑hour shifts during the week, with extended 12‑hour coverage on weekends as needed-providing consistency while supporting critical study operations. This role is ideal for nurses who prefer rotating shifts, mid shift or night work, value schedule transparency, and thrive in a focused clinical research environment.
Clinical Research Licensed Practical Nurse (LPN) / Paramedic (Multiple Shifts), Early Phase Clinical Trials - Daytona Beach, FL FortreaClinical Research Licensed Practical Nurse (LPN) / Paramedic (Multiple Shifts), Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FloridaClear Shift Structure: Work primarily 10‑hour shifts during the week, with extended 12‑hour coverage on weekends as needed—providing consistency while supporting critical study operations. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Trials - Daytona Beach, FL FortreaClinical Research Licensed Practical Nurse (LPN) / Paramedic, Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FloridaClear Shift Structure: Work primarily 10‑hour shifts during the week, with extended 12‑hour coverage on weekends as needed—providing consistency while supporting critical study operations. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Research Technician/Phlebotomist, Early Phase Clinical Research - Daytona Beach, FL Fortrea IncClinical Research Technician/Phlebotomist, Early Phase Clinical Research - Daytona Beach, FLDaytona Beach, FLAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Research Technician/Phlebotomist, Early Phase Clinical Research - Daytona Beach, FL FortreaClinical Research Technician/Phlebotomist, Early Phase Clinical Research - Daytona Beach, FLDaytona Beach, FloridaAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Pharmacist I, Early Phase Clinical Trials - Daytona Beach, FL Fortrea IncClinical Pharmacist I, Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FLIf you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Pharmacist I, Early Phase Clinical Trials - Daytona Beach, FL FortreaClinical Pharmacist I, Early Phase Clinical Trials - Daytona Beach, FLDaytona Beach, FloridaIf you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Clinical Research Feasibility Coordinator Alcanza Clinical Research LLCClinical Research Feasibility CoordinatorLake Mary, FLRequired Skills: Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm); Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc. Minimum Qualifications: A high school diploma or equivalent AND 2+ years of administrative, sales support, or similar experience, OR an equivalent combination of education and experience, is required.
Clinical Nurse Manager Florida Cancer Specialists, P.L.Clinical Nurse ManagerDeland, FLWe are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. 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.
Clinical Research Assistant / Medical Assistant Alcanza Clinical Research LLCClinical Research Assistant / Medical AssistantDeLand, 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.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorDeLand, 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;].
NewClinical Research Systems Study Build Specialist Alcanza Clinical Research LLCClinical Research Systems Study Build SpecialistLake Mary, FLReporting to the Clinical Systems Study Build Manager (or their delegate), the candidate will manage a ticketing system of requests for new builds and revisions, partner with Operations and Finance colleagues to prioritize study builds, and complete builds timely and in accordance with the study protocol. The Clinical Systems Study Build Specialist will be responsible for the creation and maintenance of financial study builds in the Clinical Trial Management System (CTMS) for the Alcanza Clinical Research site network.
Clinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorDeLand, 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;].
Clinical Nurse Manager Florida Cancer Specialists and Research InstituteClinical Nurse ManagerDeland, FLWe are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. 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.
NewClinical Research Systems Study Build Specialist Alcanza Clinical ResearchClinical Research Systems Study Build SpecialistLake Mary, FloridaRemoteReporting to the Clinical Systems Study Build Manager (or their delegate), the candidate will manage a ticketing system of requests for new builds and revisions, partner with Operations and Finance colleagues to prioritize study builds, and complete builds timely and in accordance with the study protocol. The Clinical Systems Study Build Specialist will be responsible for the creation and maintenance of financial study builds in the Clinical Trial Management System (CTMS) for the Alcanza Clinical Research site network.
Clinical Research Assistant Velocity Clinical Research IncClinical Research AssistantDaytona Beach, FLSummary: The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Director of Business Development - Clinical Research CNS/Neuro experience required Alcanza Clinical Research LLCDirector of Business Development - Clinical Research CNS/Neuro experience requiredLake Mary, FLTrack and report on business development activities: Maintain accurate records of sales activities, monitor progress against targets, and generate regular reports to senior management on business development activities, pipeline, and performance metrics. Lead business development efforts: Develop and execute business development plans, including identifying potential clients, attending conferences and industry events as needed, and leveraging existing networks to generate leads and close deals.
Clinical Research Assistant Velocity Clinical Research, Inc.Clinical Research AssistantEdgewater, FloridaTemporaryThe Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Director of Business Development - Clinical Research CNS/Neuro experience required Alcanza Clinical ResearchDirector of Business Development - Clinical Research CNS/Neuro experience requiredLake Mary, FloridaRemoteTrack and report on business development activities: Maintain accurate records of sales activities, monitor progress against targets, and generate regular reports to senior management on business development activities, pipeline, and performance metrics. Lead business development efforts: Develop and execute business development plans, including identifying potential clients, attending conferences and industry events as needed, and leveraging existing networks to generate leads and close deals.