Professor Of Clinical - Physical Therapy (Vice Chair, Research) University of MiamiProfessor Of Clinical - Physical Therapy (Vice Chair, Research)Miami, FLAccountabilities: Management and development of the PhD in Physical Therapy program in the role of Vice Chair for Research including issues related to admissions, curriculum, progression, and reporting. Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process.
Clinical 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. Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators' academic administrative personnel, and departments.
Clinical Research Nurse 2 University of MiamiClinical Research Nurse 2Miami, FLCertification and Licensing: Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration Certification in relevant specialty or field (i.e., oncology, clinical research, etc.) preferred. 2 performs all steps of the nursing process including assessing/screening of patients; interpreting data; planning, implementing, and evaluating care; coordinating care with other providers; and teaching the patient and family the knowledge and skills needed to manage their care and prevent complications while ensuring compliance with the research protocol.
Clinical Research Coordinator-Onsite Miami Jewish Health Systems IncClinical Research Coordinator-OnsiteMiami, FLServe as an initial reviewer for labs, electrocardiograms, and physical / neurological exams to identify, analyze and highlight abnormalities, liaison with subject's 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.
Clinical Research Data Specialist University of MiamiClinical Research Data SpecialistMiami, FLCollaborate with Investigators, study teams, Velos team and SCCC IT/Data team in coordinating logistics for tracking data collection, recordkeeping of participant demographic information, data entry and maintenance of databases. Participates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required.
Project Manager, Clinical Research University of MiamiProject Manager, Clinical ResearchMiami, FLCoordinate all submissions related to expanded access/compassionate use requests (single- and multi-patient) to applicable stakeholders, including but not limited to: PRMC, IRB, Office of Research Administration (ORA), other departments within University of Miami/Sylvester, ancillary committees, and U.S. Food and Drug Administration (FDA). Provide guidance to Sylvester investigators and staff related to expanded access/compassionate use requests, including but not limited to emergency use/non-emergency requests, FDA review and approval process, required committee reviews, internal workflows, etc.
Senior Clinical Research Associate - CNS - Southeast/MidAtlantic (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - Southeast/MidAtlantic (Remote)FLRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Clinical Research Nurse 1 - Plantation University of MiamiClinical Research Nurse 1 - PlantationPlantation, FLUHealth-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. The Clinical Research Nurse 1 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures.
NewSenior Clinical Research Associate IRESenior Clinical Research AssociateMiami, FloridaPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Pharmacist University of MiamiClinical Research PharmacistMiami, FLReviews adverse drug reaction follow-ups, disease state management, pharmacokinetic and lab result evaluations, drug-drug and drug-food interactions, contraindications, inappropriate therapeutic regimens, and other pharmaceutical services. Functions as key therapeutic consultant and liaison among investigators, study team, nursing and the Investigational Drug Services (IDS) Pharmacy in directing and interpreting the appropriate use of investigational products (IP).
Clinical Research Associate I - United States Thermo Fisher Scientific IncClinical Research Associate I - United StatesFL$75,000–$89,000 / yearMinimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered. What You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
Clinical Research Data Specialist (A) University of MiamiClinical Research Data Specialist (A)Miami, FLParticipates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required. 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.
Experienced Clinical Research Associate (CRA II / SR CRA)- Bilingual - US Southeast region - Multiple Therapeutic Areas Available Thermo Fisher ScientificExperienced Clinical Research Associate (CRA II / SR CRA)- Bilingual - US Southeast region - Multiple Therapeutic Areas AvailableMiami Beach, FloridaActing as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
Clinical Research Coordinator 2 (Full Time) - Ophthalmology, Bpei - Miami, FL University of MiamiClinical Research Coordinator 2 (Full Time) - Ophthalmology, Bpei - 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. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies.
Clinical Research Associate II/ Neurology/ Eastern region of the US! Thermo Fisher Scientific IncClinical Research Associate II/ Neurology/ Eastern region of the US!Miami Beach, FL$85,000–$130,000 / yearAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Clinical Research Coordinator 2 (Full Time) - Ophthalmology, BPEI - Miami, FL University of MiamiClinical Research Coordinator 2 (Full Time) - Ophthalmology, BPEI - 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. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies.
NewClinical Research Associate II IREClinical Research Associate IIFort Lauderdale, FloridaWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in West Palm Beach, FL near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Rater – Miami, FL HealthPlus StaffingClinical Research Rater – Miami, FLMiami, FloridaPosition Overview: The ideal candidate will play a crucial role in clinical trials, ensuring accurate assessments and data collection according to DSM-5 criteria. HealthPlus Staffing is assisting a prestigious client in their search for a skilled Clinical Research Rater with experience in DSM-5.
Clinical Research Associate III - 991388 Nova Southeastern UniversityClinical Research Associate III - 991388Fort Lauderdale-Davie, FLSkills: Active Listening - Proficient skills in giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Job Requirements: Required Knowledge, Skills, & Abilities: Knowledge: English Language - General knowledge of the structure and content of the English language including the meaning and spelling of words, rules of composition, and grammar.
Oncology Clinical Trials Nurse, Clinical Trials, FT, 8A-4:30P Baptist Health South FloridaOncology Clinical Trials Nurse, Clinical Trials, FT, 8A-4:30PMiami, FL$40.40–$53.73 / hourPerforms protocol specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses to the investigational treatment. ONS chemotherapy certificate must be obtained within first 6 months of employment, Association of Clinical Research Professional (ACRP) Certification or Certified Clinical Research Professional (CCRP) Certification within 1 year of employment.