UF HealthClinical Coordinator Operating Room | Florida Surgical Center | Full Time | Days UF HealthClinical Coordinator Operating Room | Florida Surgical Center | Full Time | DaysGainesville, FL$88,670.40–$151,590.40Motor Vehicle Operator Designation: Employees in this position: Will not operate vehicles for an assigned business purpose NOTE: A frequent driver is defined as one who uses his/her personal or Shands automobile a) at least once daily, b) at least five individual trips per week or c) drives, on average, over 150 miles per week in the performance of his/her job. Accountable for daily staffing and unit based follow-up of issues that assist in the assessment, planning, implementation and evaluation of patient care needs based on quality benchmarking, patient acuity/care trends, staff clinical education needs and patient satisfaction.
HCA Florida North Florida HospitalRN Patient Safety Coordinator HCA Florida North Florida HospitalRN Patient Safety CoordinatorGainesville, FLIn an effort to increase patient satisfaction and reduce liabilities and exposures for the facility, this position will establish, coordinate and manage Patient Safety education initiatives which include, but are not limited to, new employees in orientation, current employees, visitors and students doing clinical rotations in the facility. Our hospital has an Accredited Chest Pain Center by ACC (American College of Cardiology) and is designated as a Blue Distinction Center for Spine Surgery and Bariatric Surgery.
HCA Florida North Florida HospitalClinical Nurse Coord Intermediate Care Unit HCA Florida North Florida HospitalClinical Nurse Coord Intermediate Care UnitGainesville, FLAdditional 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.
HCA Florida Memorial HospitalRN Trauma Performance Improvement Coordinator HCA Florida Memorial HospitalRN Trauma Performance Improvement CoordinatorJacksonville, FLMemorial Hospital has provided quality healthcare services since 1969, giving patients access to highly-trained physicians and advanced technology. Other specialized programs include our accredited Chest Pain Center, certified Stroke Center, Heart Center, Bone and Joint Center, maternity center and much more.
The Medicus FirmAcademic Bone Marrow Transplant in Florida The Medicus FirmAcademic Bone Marrow Transplant in FloridaGainesville, FLThis is a rare opportunity to combine high-impact clinical care with cutting-edge clinical trials and translational research in hematologic malignancies, stem cell transplantation, and cellular immunotherapy. A prestigious university in Gainesville, FL is actively seeking a Bone Marrow Transplant (BMT) physician to join its expanding, FACT-accredited transplant program.
University of MiamiClinical Research Coordinator 3 University of MiamiClinical Research Coordinator 3miami, FLCore Qualifications Bachelor's degree in relevant field required Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months Minimum 4 years of relevant experience required Knowledge, Skills and Attitudes: Skill in collecting, organizing and analyzing data. This role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators.
University of MiamiClinical Research Coordinator 3 (A) University of MiamiClinical Research Coordinator 3 (A)Miami, FLThis role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators. The Clinical Research Coordinator 3 (A) serves as an experienced clinical research professional responsible for providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols.
Inspire Path Networks, LLCSenior Clinical Research Coordinator – Hematology/Oncology Inspire Path Networks, LLCSenior Clinical Research Coordinator – Hematology/OncologyMiami, FloridaThis is a fully onsite position located on the main corporate campus and is ideal for an experienced research professional who is comfortable managing high-enrollment studies and complex clinical trial activities. Clinical Research Coordinator will independently manage the day-to-day operations of assigned studies while ensuring compliance with study protocols, GCP guidelines, IRB requirements, and FDA regulations.
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR II H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR IITampa, FLCredentials and Qualifications: • Bachelor's degree with 2 years clinical trials coordination experience • In lieu of a bachelor's degree, an associate's degree with 4 years clinical trials coordination experience may be considered • CCRP/CCRC certification preferred. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities.
Nicklaus Children's HospitalSr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days)Miami, FLBeyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities. Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study.
AdventHealthClinical Research Coordinator II Orlando Onsite AdventHealthClinical Research Coordinator II Orlando OnsiteOrlando, FL$49,307.53–$91,705.34 / yearDetail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties Other duties as assigned. Additional Information: An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement: - Bachelors degree and 2+ years of experience OR - Associates degree and 4+ years of experience OR - Technical/Vocational School and 6+ years of clinical research experience.
AdventHealthClinical Research Coordinator II AdventHealthClinical Research Coordinator IIWinter Park, FL$49,307.53–$91,705.34 / yearDetail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties Other duties as assigned. Additional Information: An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement: - Bachelors degree and 2+ years of experience OR - Associates degree and 4+ years of experience OR - Technical/Vocational School and 6+ years of clinical research experience.
Care AccessNewClinical Research Coordinator III Care AccessClinical Research Coordinator IIITampa, FloridaWith 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.
Cardiovascular Associates of AmericaNewRN or LPN Clinical Research Coordinator Cardiovascular Associates of AmericaRN or LPN Clinical Research CoordinatorPalm Beach Gardens, FloridaPosition Overview: As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. About CVAUSA: Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes.
Care Access Research LLCClinical Research Coordinator III Care Access Research LLCClinical Research Coordinator IIITampa, FL$65,000–$95,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
University of FloridaClinical Research Coordinator III University of FloridaClinical Research Coordinator IIIGainesville, FL$60,000–$82,000 / yearThe Clinical Research Coordinator III must be able to perform the following essential just functions independently for multiple ongoing clinical trials: Serve as study coordinator for clinical trial protocols as assigned: Activities include and are not limited to: recruiting patients to enroll in study(ies); coordinating patient visits; managing patient visits in accordance to protocol; coordinating site monitor visits; submitting necessary compliance paperwork; ensuring billing compliance; resolving issues/questions with the sponsor; serving as the liaison between the Principal Investigator and study subjects; performing study feasibility assessments for potential new studies. Clinical trial regulatory compliance management: Activities included but are not limited to: initiating and maintaining a current regulatory file; preparing and submitting documents related to clinical trials to both internal (UF-IRB, UF-OCR, UF-IBC, etc.) and external (FDA, RAC, WIRB, etc) organizations as required; completing end of study procedures; scheduling and participating in sponsored research monitoring visits; assuring that the clinical research trial''''s integrity and quality are maintained and that the trial is conducted following Good Clinical Practice guidelines; attending UF-IRB 01 full board meetings as necessary.
Actalent IncSr. Clinical Research Coordinator Actalent IncSr. Clinical Research CoordinatorMiami, FL$32–$43 / hourClinical Research Coordinator (SCRC) ensures that clinical studies are conducted in accordance with the protocol, applicable regulations, Good Clinical Practice (GCP), and Institutional Review Board (IRB) requirements. 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.
AdventHealthClinical Research Coordinator I RN AdventHealthClinical Research Coordinator I RNOrlando, FL$65,582.40–$108,646.85 / yearKnowledge, Skills, and Abilities: Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice. Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required].
H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute IncCLINICAL RESEARCH COORDINATOR ITampa, FLThese positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities.
GULF COAST HEART AND VASCULAR LLCClinical Research Coordinator - Part Time GULF COAST HEART AND VASCULAR LLCClinical Research Coordinator - Part TimePanama City, FLThe CRC will be responsible for the day-to-day coordination and execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP). Accurately document study data in source documents and electronic data capture (EDC) systems .
University of FloridaNewClinical Research Coordinator I University of FloridaClinical Research Coordinator IGainesville, FL$46,000–$48,000 / yearResearches regulatory compliance participation in activities to initiate and maintain a current regulatory file; prepares and submits documents related to research protocols to both internal (UF-IRB, UF-CTC office, UF-OCR, etc.) and external (FDA, WIRB, etc.) organizations as required; completes end-of-study procedures; schedules and participates in sponsored research monitoring visits and QA audits; ensures the integrity and quality of the research protocol is maintained and the trial is conducted in accordance with GCP guidelines; attends UF-IRB 01 full board meetings as necessary. Job Description:Selects and recruits study participants to enroll in various studies and protocols; participates in the informed consent process of study subjects; supports the safety of clinical research patients/research participants; coordinates protocol-related research procedures, study visits, and follow-up care; screens, completes case report forms (paper & electronic data capture), and addresses queries.
Cardiovascular Associates of AmericaClinical Research Coordinator Cardiovascular Associates of AmericaClinical Research CoordinatorOrlando, FloridaPosition Overview: As a Clinical Research Coordinator you will play a key role in managing and overseeing all aspects of clinical trials and site operations. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide.
Florida Cancer Specialists and Research InstituteClinical Research Coordinator III Drug Development Unit Florida Cancer Specialists and Research InstituteClinical Research Coordinator III Drug Development UnitSarasota, FLMay 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.
AdventHealthClinical Research Coordinator II RN Oncology AdventHealthClinical Research Coordinator II RN OncologyAltamonte Springs, FL$65,582.40–$108,646.85 / yearLicenses and Certifications: • Registered Nurse (RN) [Required] • Basic Life Support - CPR Cert (BLS) [Required] • Advanced Cardiac Life Support Cert (ACLS) [Preferred] • Certified Clinical Research Professional (SOCRA) (CCRP) [Preferred] • Certified Clinical Research Coordinator (CCRC) [Preferred] • Oncology Certified Nurse (OCN) [Preferred]. Schedule: Full time Shift: Day (United States of America) Address: 601 E ALTAMONTE DRIVE City: ALTAMONTE SPRINGS State: Florida Postal Code: 32701.
AdventHealthClinical Research Coordinator II RN AdventHealthClinical Research Coordinator II RNOrlando, FL$65,582.40–$108,646.85 / yearLicenses and Certifications: • Registered Nurse (RN [Required] • Basic Life Support - CPR Cert (BLS [Required] • Advanced Cardiac Life Support Cert (ACLS [Preferred] • Certified Clinical Research Professional (SOCRA [Preferred] • Certified Clinical Research Coordinator (CCRC [Preferred] • Oncology Certified Nurse (OCN [Preferred]. • Interpersonal communication skills; ability to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances.
ECN Operating LLCClinical Research Coordinator ECN Operating LLCClinical Research CoordinatorJacksonville, FLThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.
AdventHealthClinical Research Coordinator I- RN AdventHealthClinical Research Coordinator I- RNOrlando, FL$65,582.40–$108,646.85 / yearAbility to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. Works flexible hours and is available for research project-related questions Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
Headlands Research IncClinical Research Coordinator Headlands Research IncClinical Research CoordinatorLake Worth, FLEducation & Experience Requirements: • High school diploma or GED • Minimum of 1 year of experience as a Clinical Research Coordinator • Minimum of 2 years of college within a health-related program • Licensed as a Licensed Practical Nurse (LPN) or higher • Bachelor's degree in a health or scientific-related program. • Skills & Qualifications: • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures • Proficiency in medical terminology and clinical documentation practices • Strong interpersonal, verbal, and written communication skills • Organized, detail-oriented, and capable of managing multiple priorities • Proficient in Microsoft Office and other clinical research systems.
Metabolic Research Institute IncClinical Research Coordinator Metabolic Research Institute IncClinical Research CoordinatorWest Palm Beach, FL$26–$28 / hourMetabolic Research Institute (MRI) is seeking an experienced Clinical Research Coordinator to join our dynamic and growing team. We are a respected private clinical research organization dedicated to advancing science and improving lives through innovative studies in diabetes and metabolic health.
Mount Sinai Medical Center of FloridaClinical Research Coordinator Mount Sinai Medical Center of FloridaClinical Research CoordinatorMiami Beach, FloridaWe offer the latest in advanced medicine, technology, and comfort in 12 facilities across Miami-Dade (including our 674-bed main campus facility) and Monroe Counties, with 38 medical services, including cancer care, 24/7 emergency care, orthopedics, cardiovascular care, and more. Reviews charts of patients who are referred for studies and ensures that all protocol required tests are ordered and performed; makes sure that all eligibility criteria are met.
University of MiamiClinical Research Coordinator 1 University of MiamiClinical Research Coordinator 1miami, FLClinical Research Coordinator 1The University of Miami/UHealth department of The Sylvester Comprehensive Cancer Center(SCCC) has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work on the UHealth Campus. UHealth-University of Miami Health System, South Florida''s only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine.
University of MiamiClinical Research Coordinator 2 University of MiamiClinical Research Coordinator 2Miami, FLThe incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel. Importantly, this CRC2 role will be dedicated to federally funded studies in areas such as cognitive impairment and schizophrenia, where accurate data collection, strict regulatory compliance, and careful participant oversight are essential to advancing the department's research mission.
Miami Jewish Health Systems IncClinical Research Coordinator Miami Jewish Health Systems IncClinical Research CoordinatorMiami, FLServe as an initial reviewer for labs, electrocardiograms, and physical / neurological exams to identify, analyze and highlight abnormalities, liaison with subjects primary care physicians for follow-up and present all findings to the PI for review and signature. Our main campus is located on 20+ acres just north of mid-town Miami, and is home to our support departments like Finance, Accounting, Human Resources, Marketing and more.
CAREERXCHANGE, Inc.NewSr Clinical Research Coordinator CAREERXCHANGE, Inc.Sr Clinical Research CoordinatorMiami, FL$32–$43 / hourThis role is responsible for coordinating all aspects of clinical research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while delivering exceptional patient care. Job SummaryWe are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15-week contract assignment.
ObjectiveHealth IncClinical Research Coordinator I ObjectiveHealth IncClinical Research Coordinator IOcala, FLNot easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
University of MiamiClinical Research Coordinator 1 (A) University of MiamiClinical Research Coordinator 1 (A)Miami, FLBachelors degree in relevant field required • Minimum 1 year of relevant experience required • Bilingual in English and Spanish highly desired • Phlebotomy certification highly desired, or requires completion of a formal Phlebotomy training program within 30 days of hire. UHealth-University of Miami Health System, South Floridas only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine.
Flourish ResearchClinical Research Coordinator - Bilingual Flourish ResearchClinical Research Coordinator - BilingualLeesburg, FloridaFlourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
University of FloridaClinical Research Coordinator II - UF Emergency Medicine University of FloridaClinical Research Coordinator II - UF Emergency MedicineGainesville, FL$53,000–$60,000 / yearThe Clinical Research Coordinator II will work collaboratively with the Vice Chair of Research, Principal Investigators (PIs), the Clinical Research Manager, research administrators, coordinators, sponsors, and institutional partners to ensure all research activities are conducted in accordance with federal regulations, University of Florida policies, and sponsor requirements. This position plays a vital role in coordinating and managing clinical research activities across all phases of study operations, including regulatory submissions, participant recruitment and enrollment, study implementation, data collection, compliance monitoring, reporting, and project closeout.
Teva Pharmaceutical Industries LtdNewClinical Research Coordinator Floater - 2nd & 3rd Shift Teva Pharmaceutical Industries LtdClinical Research Coordinator Floater - 2nd & 3rd ShiftMiramar, FLAdditional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Provides ongoing assessment of the study subject/patient to identify Adverse Events (AEs), ensures proper documentation and reporting of all AEs, including follow up of open AES when subjects are not in-house, and provides any appropriate clinical care or instructions to subjects, as directed by the PI or as deemed medically necessary by their professional judgment.
Actalent IncPart-Time Clinical Research Coordinator Actalent IncPart-Time Clinical Research CoordinatorNaples, FL$25–$33 / hourYou will focus on accurate data entry, query resolution, and effective communication about the clinical trial, helping ensure the integrity and quality of study data while supporting patient-centered research activities. 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.
Actalent IncMiami, FL- Clinical Research Coordinator Actalent IncMiami, FL- Clinical Research CoordinatorMiami, FL$25–$32 / hourIf 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. You will need to perform effective communication about the clinical trial, spread study awareness in the community, and conduct patient-centered research activities.
University of MiamiClinical Research Coordinator 2 (A) Full Time Bascom Palmer Eye Institute Miami, FL University of MiamiClinical Research Coordinator 2 (A) Full Time Bascom Palmer Eye Institute Miami, FLMiami, FLThe incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel. Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators' academic administrative personnel, and departments.
University of MiamiClinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FL University of MiamiClinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FLMiami, FLCoordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine.
University of MiamiClinical Research Coordinator 1 (A) Full Time Bascom Palmer Eye Institute Miami, FL University of MiamiClinical Research Coordinator 1 (A) Full Time Bascom Palmer Eye Institute Miami, FLMiami, FLCoordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine.
Actalent IncClinical Research Coordinator Actalent IncClinical Research CoordinatorHollywood, FL$32–$36 / hourThis position focuses on research participant recruitment and consenting, delivering concierge-level service throughout the clinical trial journey, and coordinating biospecimen collection in collaboration with clinical research nursing, laboratory teams, and hospital departments. The Clinical Research Coordinator II (Non-RN) plays a key role in all aspects of clinical research, including screening and enrolling participants, coordinating their care and follow-up, and ensuring strict adherence to regulatory and protocol requirements.
Headlands ResearchNewClinical Research Coordinator Headlands ResearchClinical Research CoordinatorLake Worth, FloridaAs a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
Actalent IncBilingual Clinical Research Coordinator Actalent IncBilingual Clinical Research CoordinatorHollywood, FL$28–$33 / hourIf 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. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
Mayo ClinicAssociate Clinical Research Coordinator for Women's Health Mayo ClinicAssociate Clinical Research Coordinator for Women's HealthJacksonville, FL$24.55–$35.65 / hourMinimum Education and/or Experience Required: (Education Requirements and Experience): HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate Program with at least 1 year of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's degree. Position Overview: (Major Functions and Non-Essential Functions): Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
Alcanza Clinical ResearchNewClinical Research Source Development Coordinator Alcanza Clinical ResearchClinical Research Source Development CoordinatorLake Mary, FloridaRemoteInitial creation of source documents will use all available protocol specific documents (i.e., current IRB approved protocol, blank or annotated CRF, Sponsor provided source templates/worksheets, or reference manuals) to create a source document that is accurate and complete and to ensure that the source document is equipped to record all the required data for the visit. Position Summary: The Clinical Source Development Coordinator is an integral part of the Clinical team and will work closely with the Site teams and other key stakeholders in designing, updating, controlling, and releasing source (electronic or paper) for clinical trials.
Alcanza Clinical ResearchClinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorClearwater, FloridaScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].