Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Metabolic - US Any RegionFLWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Associate (CRA II/Senior) - Ophthalmology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Ophthalmology - US Any RegionFLWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Lead Clinical Research Coordinator - Cancer Institute (Full Time, Days) Nicklaus Children's HospitalLead Clinical Research Coordinator - Cancer Institute (Full Time, Days)Miami, FLUnder direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children''s Research Institute. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities.
Lead Clinical Research Coordinator (Full Time, Days) Nicklaus Children's HospitalLead Clinical Research Coordinator (Full Time, Days)Miami, FLUnder direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children's Research Institute. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities.
Clinical Research Associate II Becton Dickinson Medical DevicesClinical Research Associate IIMiami, FloridaIndependently Conduct on-site or remote clinical site monitoring activities for assigned clinical sites to evaluate sites for qualification or activation, review informed consent forms, review subject data for accuracy, issue and address data queries, ensure study is conducted compliantly, address/escalate study non-compliance issues, verify that any corrective actions are implemented, perform investigational clinical product accountability, ensure proper regulatory approval, review essential clinical study documents for completion/accuracy, conduct study training/presentations, ensure proper training documentation, ensure timely reporting for reportable events (e.g., Unanticipated Adverse Device Effects, device deficiencies, etc.), ensure good documentation/clinical practices (GDP/GCP), ensure study supplies are adequate and perform other site management & monitoring activities, as needed. Develop and/or complete study-specific Clinical Site Activation Checklists, Master Site Selection Trackers, Qualification Visit Reports, Initiation Visit Reports, Interim Monitoring Visit Reports, Close-Out Visit Reports, Confirmation & Follow-Up Letters, Clinical Site Product Accountability Logs, Clinical Site Training Logs, Clinical Site Visit Logs, Delegation of Authority Logs, Clinical Monitoring Plans, Financial Disclosure Forms and other essential clinical study documents, as needed.
Sr. 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.
Sr. Clinical Research Coord. - Oncology (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coord. - Oncology (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.
Assistant Professor Of Clinical - Medical Oncology / Genitourinary University of MiamiAssistant Professor Of Clinical - Medical Oncology / GenitourinaryDoral, FLPosition Requirements: Qualifications should include a demonstrated track record of excellence in patient care, research, peer-reviewed publications, and the potential to serve as principal investigator of cutting-edge clinical trials. Explore and develop appropriate research collaborations both within and outside the Sylvester Comprehensive Cancer Center or the University of Miami Miller School of Medicine departments and schools.
Assistant Professor of Clinical - Medicine, Medical Oncology University of MiamiAssistant Professor of Clinical - Medicine, Medical OncologyNorth Miami, FloridaQualifications should include a demonstrated track record of excellence in patient care, research, peer-reviewed publications, and the potential to serve as principal investigator of cutting-edge clinical trials. Explore and develop appropriate research collaborations both within and outside the Sylvester Comprehensive Cancer Center or the University of Miami Miller School of Medicine departments and schools.
Assistant Professor of Clinical - Neurology, Neuromuscular University of MiamiAssistant Professor of Clinical - Neurology, NeuromuscularMiami, FloridaThe incumbent will be appointed at the rank of non-tenure earning Assistant Professor on the clinical educator track in the Neuromuscular Division, Department of Neurology at the University of Miami School of Medicine. The Department of Neurology at the University of Miami, Miller School of Medicine has an exciting opportunity for a full time Assistant Professor of Clinical Neurology in the Neurology Neuromuscular Division.
Associate Director, Pediatric Clinical Research (Md/Do) - Cancer Institute Nicklaus Children's HospitalAssociate Director, Pediatric Clinical Research (Md/Do) - Cancer InstituteMiami, FLThe Associate Director of Pediatric Clinical Research - Cancer Center, serves as the senior operational and execution leader for all pediatric cancer clinical research activities within the Cancer Center, including early phase (Phase I/first in child), investigator initiated, cooperative group, and sponsor driven trials supported by the CORKK and Cancer Center grant portfolio. Provides oversight and scientific direction in protocol development, translational integration, data interpretation, regulatory documentation, and dissemination of research findings, while retaining responsibility for operations, performance, governance, and program execution.
Lead Clin Research Coordinator (Full Time, Days) Nicklaus Children's HospitalLead Clin Research Coordinator (Full Time, Days)Miami, FLUnder direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator CTO will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children''s Research Institute. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities.
Sr. Research Compliance Specialist (Full Time, Days) Nicklaus Children's HospitalSr. Research Compliance Specialist (Full Time, Days)Miami, FLThe position provides advanced, subject-matter-expert-level compliance guidance, mentors junior compliance staff, and drives continuous quality improvement by identifying compliance risks, coordinating corrective and preventive actions, and partnering with the research education team to maintain audit readiness and regulatory compliance across the research portfolio. This role independently leads internal auditing and preparatory audit activities and serves as the primary liaison for FDA audits and other external regulatory inspections, partnering with study teams to resolve compliance concerns identified during sponsor monitoring visits.
Research Contract Specialist (Full Time, Days) Nicklaus Children's HospitalResearch Contract Specialist (Full Time, Days)Miami, FLOversees and coordinates day to day administrative functions associated with the contracting process within organization's Human Research Protections Program (HRPP) at the Research Institute and the Office of Sponsored Programs (OSP). Performs initial and ongoing review and provides comments on contractual agreements received from clients and suppliers including AAHRPP language.
Senior Clinical Research Associate - Psychiatry - Southeast Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - SoutheastFL$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.
Sr. Research Nurse (Full Time, Days) Nicklaus Children's HospitalSr. Research Nurse (Full Time, Days)Miami, FLThis research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA's, Study Team (PI, Sub-I's, CRC', etc.), NCH-RI departments and Nicklaus Children's Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements. Implements, monitors, and assesses the need for training programs to maintain staff skill proficiency, including annual validation and currency of required certifications and licenses.
Sr. Research Nurse - Cancer Institute (Full Time, Days) Nicklaus Children's HospitalSr. Research Nurse - Cancer Institute (Full Time, Days)Miami, FLThis research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA''s, Study Team (PI, Sub-I''s, CRC'', etc.), NCH-RI departments and Nicklaus Children''s Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements. Implements, monitors, and assesses the need for training programs to maintain staff skill proficiency, including annual validation and currency of required certifications and licenses.
Sr. Research Nurse - Cancer Institute - Ft. Lauderdale Nicklaus Children's HospitalSr. Research Nurse - Cancer Institute - Ft. LauderdaleMiami, FLThis research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA''s, Study Team (PI, Sub-I''s, CRC'', etc.), NCH-RI departments and Nicklaus Children''s Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements. Implements, monitors, and assesses the need for training programs to maintain staff skill proficiency, including annual validation and currency of required certifications and licenses.
Sr. Research Regulatory Specialist (Full Time, Days) Nicklaus Children's HospitalSr. Research Regulatory Specialist (Full Time, Days)Miami, FLThis position also applies experience using a clinical trial management system (CTMS) and electronic regulatory systems for protocol and regulatory document management, with responsibility for creating, maintaining, and scheduling portfolio reports that keep key stakeholders informed of study progress, regulatory milestones, risks, and overall portfolio status. The Senior Research Regulatory Specialist applies advanced experience supporting Phase 1 research, Independent Review Board (IRB), Institutional Biosafety Committee (IBC) submissions, and a broad range of institutional research committee reviews to guide complex study activation and ongoing regulatory maintenance.
RN Clinical Services Group Manager Becton Dickinson Medical DevicesRN Clinical Services Group ManagerMiami, FloridaUSA DC - Washington, DC, USA FL - Miami, USA MO - St Louis, USA MT - Bozeman, USA OH - Cleveland, USA TX - Austin, USA TX - San Antonio, USA UT - Salt Lake City, USA WA - Seattle Work Shift. Bachelor's Degree in Healthcare Administration, Nursing, or related field, with 8 years of previous related experience with direct healthcare management of large clinical organizations required.