Supervisor Clinical Research Coordinator (Orthopedics) Rady Children's HealthSupervisor Clinical Research Coordinator (Orthopedics)Orange, CAStudy management includes but is not limited to assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, coordinating and collecting research data/specimens, completing study records in an accurate and timely manner, participating in quality assurance audits, managing study materials and supplies, communicating across multiple teams, and archiving records in accordance with appropriate policies and procedures. Physical Activity Requirements: Bending, Carry Objects, Climbing, Keyboard use/repetitive motion, Pinching/fine motor activities, Push/Pull, Reaching forward, Reaching overhead, Sitting, Squat/kneel/crawl (Squad & Knee), Standing, Talk or hear, Taste or smell, Twisting, Walking, Wrist position deviation.
Research Associate III - Ajami Lab - Department of Neurology Cedars-Sinai Medical CenterResearch Associate III - Ajami Lab - Department of NeurologyLos Angeles, CACedars-Sinai offers scientists unparalleled access to ground breaking technologies, facilities, and resources for conducting research related to an impressive range of diseases and disorders, from cancer, cardiology, and digestive diseases, to genetics, genomics, neurosciences, and women's health. The incumbent may be requested by PI to take on specific supervisory activities, provide administrative leadership and/or technical expertise, may develop hypothesis, assists in planning steps for the investigative process, and will review and remain current on literature as it relates to clinical/research study.
Pediatrics Developmental & Stem Cell Biology - Assistant Professor (Cedars-Sinai Research Scientist I) Cedars-Sinai Medical CenterPediatrics Developmental & Stem Cell Biology - Assistant Professor (Cedars-Sinai Research Scientist I)Los Angeles, CA$71,094–$235,019 / yearExamples include investigating how high-fat diets may promote liver cancer as well as the effects of near weightlessness on iPSCs in conjunction with NASA, connections among diabetes and chronic pancreatitis and pancreatic cancer, and the genetic underpinnings of disease, exploiting the potential of stem cells, leveraging nanotechnology, parsing big data, and assessing how gender and metabolism impact health. The Department of Pediatrics at Cedars-Sinai Guerin Children's is recruiting an independent Research Scientist faculty member (Assistant Professor faculty rank) to join a new Center specializing in Developmental and Stem Cell Biology.
Clinical Research Coordinator III (Hybrid) Cedars-Sinai Medical CenterClinical Research Coordinator III (Hybrid)Beverly Hills, CAThe Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Senior Clinical Research Associate - CNS/Rare Disease - West Coast Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Rare Disease - West CoastCA$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.
Senior Clinical Research Associate - Psychiatry - West Coast (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - West Coast (Remote)CARemote$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 Associate TalentBurst, Inc.Clinical Research AssociateIrvine, CA$45–$55 / hourConduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. The main function of a clinical research specialist is to perform study start-up and conduct activities, including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.
Clinical Research Coordinator I - Heart Institute - Bairey-Merz Lab Cedars-Sinai Medical CenterClinical Research Coordinator I - Heart Institute - Bairey-Merz LabLos Angeles, CAThe Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
Clinical Research Associate II Cedars-Sinai Medical CenterClinical Research Associate IILos Angeles, CADr. Tan, Associate Professor, Cancer Research Center for Health Equity, Division of Population Sciences, Department of Biomedical Sciences, is a social psychologist and applies her training in behavioral and prevention sciences to develop innovative interventions for improving health outcomes among marginalized populations in the U.S. This position provides contributions to behavioral and implementation science for the Cancer Research Center for Health Equity. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.
Heart Institute - Clinical Research Data Specialist I, Susan Cheng Team Cedars-Sinai Medical CenterHeart Institute - Clinical Research Data Specialist I, Susan Cheng TeamLos Angeles, CAWith over 450 peer-reviewed publications in prestigious journals such as JAMA, Circulation, and The New England Journal of Medicine, Dr. Cheng's work has significantly advanced understanding in her field. Her leadership in clinical research is exemplified by founding the largest COVID-19 clinical research program on the West Coast during the early stages of the pandemic.
Clinical Research Coordinator I - Kidney Transplant Cedars-Sinai Medical CenterClinical Research Coordinator I - Kidney TransplantCalifornia, CAThe Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Principal Responsibilities: Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
Clinical Research Coordinator II National InstituteClinical Research Coordinator IIGarden Grove, California$24–$32 / hourNICR provides sponsors and CROs premium services leading to rapid study site identification, trial placement, site initiation, and successful subject enrollment. Who We Are From our roots in Nephrology, we have expanded into many other specialty fields, including cardiometabolic, infectious diseases, geriatrics, and many other challenging & underserved areas of healthcare.
Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite) Medtronic PlcSenior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite)Irvine, CAIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
Clinical & Research Fellow – Ophthalmology NVISION Eye CentersClinical & Research Fellow – OphthalmologyTorrance, CaliforniaInternAlongside clinical training, the position features a structured educational curriculum including didactic lectures and an interactive journal club to prepare the candidate for medical school or advanced graduate programs. Diagnostic Testing: Measure visual acuity, perform lensometry, test intraocular pressure (tonometry), and run advanced imaging such as Optical Coherence Tomography (OCT) and visual field analyzers.
Research Assistant - Student Worker Northcentral UniversityResearch Assistant - Student WorkerCACurrent work will support the United 4 Youth (U4Y) Learning and Evaluation Project, a collaborative, equity-centered initiative focused on improving outcomes for youth through systems alignment, data-informed decision-making, and continuous learning. We are united in our mission to meet the global education demands of the 21st Century and are dedicated to creating a supportive academic and work environment that allows students, faculty and staff to develop their interests and talents while experiencing a sense of community.
Clinical Research Coordinator II - Clinical Trials Cedars-Sinai Medical CenterClinical Research Coordinator II - Clinical TrialsLos Angeles, CA$28.86–$49.06 / hourReq ID 19843 Working Title Clinical Research Coordinator II - Clinical Trials Department Cancer - SOCCI Clinical Research Business Entity Cedars-Sinai Medical Center Job Category Academic / Research Job Specialty Research Studies/ Clin Trial Overtime Status EXEMPT Primary Shift Day Shift Duration 8 hour Base Pay $28.86 - $49.06. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology Cedars-Sinai Medical CenterClinical Research Associate I - Karsh Division of Gastroenterology and HepatologyLos Angeles, CA$25–$33.51 / hourReq ID 20668 Working Title Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology Department Research - General Medicine Business Entity Cedars-Sinai Medical Center Job Category Academic / Research Job Specialty Research Studies/ Clin Trial Overtime Status NONEXEMPT Primary Shift Day Shift Duration 8 hour Base Pay $25.00 - $33.51. Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Clinical - Assoc Spec, Clinical Research MindlanceClinical - Assoc Spec, Clinical Researchirvine, CA$43.56–$45.37 / hourConduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. Summary: The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.
Clinical Research Recruitment Coordinator Irvine Clinical ResearchClinical Research Recruitment CoordinatorIrvine, CAIrvine Clinical Research is looking for a friendly, outgoing person to join our team as a Clinical Research Recruitment Coordinator. Recruit study participants via short telephone interviews; make outbound phone calls to achieve appointment scheduling goal.
Senior Clinical Research Associate PSI CRO AGSenior Clinical Research AssociateCAAdvance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred.