Clinical Research Specialist I - Oncology & Clinical Research Cedars-Sinai Medical CenterClinical Research Specialist I - Oncology & Clinical ResearchLos Angeles, CAYou'll stand out if you also have experience in oncology research, biobanking, or molecular research initiatives, along with exposure to protocol development, investigator-initiated studies, laboratory operations supporting clinical trials, reporting, database management, or process improvement and automation initiatives. You should have experience working with biological specimens (collection, processing, storage, or shipment), be familiar with Good Clinical Practice (GCP) and clinical research regulations, and have strong organizational skills with the ability to manage multiple priorities.
NewResearch Nurse Coordinator II (10HR/Full-Time) - The Angeles Clinic & Research Institute - $10,000 Sign On Bonus! Cedars-Sinai Medical CenterResearch Nurse Coordinator II (10HR/Full-Time) - The Angeles Clinic & Research Institute - $10,000 Sign On Bonus!Los Angeles, CAThe Research Nurse Coordinator II is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. The Angeles Clinic and Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateLos Angeles, CA$110,520–$138,150 / yearWilling and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, 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.
Game Research & Development Intern, Engine Research 107344 Tencent Holdings LtdGame Research & Development Intern, Engine Research 107344Los Angeles, CA$28.27–$60 / hourWhat the Role Entails Working with scientists to research and develop advanced techniques in the following topics: 3D geometric learning, Re-meshing and UV optimization, Physically-based animation and simulation Machine learning for computer graphics Motion planning in virtual city Character locomotion and control realistic image synthesis and real-time rendering techniques Researching and developing tools and pipelines to facilitate the use of technologies in the game development environment Who We Look For Strong coding skills in one of following programming languages: C++, python, TensorFlow/Torch Solid knowledge in calculus, linear algebra, basic numerical analysis A strong sense of responsibility and good communication skills Plus: Graduate students in a master or Ph. D. level program Publications on computer graphics/vision, machine learning, and robotics Familiarity with game engine, graphics APIs, and GPU programming Location State(s) US-California-Los Angeles The expected base pay range for this position in the location(s) listed above is $28.27 to $60.00 per hour.
NewResearch Healthcare Lead - Research & Strategy Clarion PartnersResearch Healthcare Lead - Research & StrategyLos Angeles, Louisiana$15,000–$25,000 / yearReporting to the Global Head of Research & Strategy, this highly visible role works closely with senior stakeholders across Portfolio Management, Transactions, Asset Management, and Client Capital Management, as well as directly with a dedicated data science team. Support deal teams by developing, validating, and documenting healthcare-specific underwriting assumptions (e.g., demand drivers, payor mix, reimbursement sensitivity, labor costs, and operating margin trends) for acquisitions, developments, and platform investments.
Senior Clinical Research Associate IRESenior Clinical Research AssociateLos Angeles, California$110,520–$138,150 / yearPerform 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- Los Angeles, CA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Internal Medicine - Clinical Research Investigator ECN Operating LLCInternal Medicine - Clinical Research InvestigatorNorthridge, CA$150–$250 / hourThe ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator , while continuing to provide high-quality medical care to adult patients within a clinical research setting. Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Internal Medicine - Clinical Research Investigator in Northridge, California to join our expanding team of clinical professionals.
NewClinical Research Budgeting Analyst - Clinical Trials Providence St. Joseph HealthClinical Research Budgeting Analyst - Clinical TrialsLos Angeles, CARemoteMain responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budget milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments. The Clinical Research Budgeting Analyst will be responsible for the timely and accurate preparation and maintenance of budgets for sponsored clinical trials, including the comparative review against budgets offered by study sponsors and the set-up of study payments milestones in the Clinical Trial Management System.
NewResearch Nurse IV, Clinical Trials LVN (Durational with Benefits) Kaiser PermanenteResearch Nurse IV, Clinical Trials LVN (Durational with Benefits)Los Angeles, CAConducts and leads clinical research by: reviewing, designing, and collecting clinical trials data; leveraging an advanced knowledge of source data and the tools leveraged for analyzing, and interpreting clinical data; leveraging advanced knowledge when providing input on the design of clinical trials, studies, and interventions at the site-level; developing innovative clinical research protocols and other processes of large-scale clinical trials; preparing, submitting, and/or collaborating with others to ensure correct compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for executing clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in various research lab operations (e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). Ensures documentation of clinical research files by: ensuring the timely, accurate, and complete documentation of all research activities (e.g., consent forms, reports, tracking forms); contributing to the development and/or implementation of moderately complex quality control and/or assurance measures and providing feedback to research staff and management; assessing volunteers and/or patients for eligibility to participate in Clinical Trials, escalating when necessary; and monitoring and auditing Clinical Trials across sites and presenting findings to KP leadership.
Research Nurse IV, LPN/LVN, Clinical Trials Kaiser PermanenteResearch Nurse IV, LPN/LVN, Clinical TrialsLos Angeles, CAConducts and leads clinical research by: reviewing, designing, and collecting clinical trials data; leveraging an advanced knowledge of source data and the tools leveraged for analyzing, and interpreting clinical data; leveraging advanced knowledge when providing input on the design of clinical trials, studies, and interventions at the site-level; developing innovative clinical research protocols and other processes of large-scale clinical trials; preparing, submitting, and/or collaborating with others to ensure correct compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for executing clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in various research lab operations (e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). Ensures documentation of clinical research files by: ensuring the timely, accurate, and complete documentation of all research activities (e.g., consent forms, reports, tracking forms); contributing to the development and/or implementation of moderately complex quality control and/or assurance measures and providing feedback to research staff and management; assessing volunteers and/or patients for eligibility to participate in Clinical Trials, escalating when necessary; and monitoring and auditing Clinical Trials across sites and presenting findings to KP leadership.
Clinical Research Coordinator III Children's Hospital Los AngelesClinical Research Coordinator IIILos Angeles, California$81,120–$108,160 / yearFull timeThe role also provides cross-coverage for other Clinical Research Coordinators, trains and mentors new staff, develops and improves clinical trial coordination procedures, and ensures the effective management, compliance, and execution of complex research protocols across the Transplant and Cellular Therapy research portfolio. Serving as a key resource for Principal Investigators, faculty, and study team members, this role oversees a diverse portfolio of research studies, including CAR T-cell therapy, gene therapy, other therapeutic treatment trials, observational studies, and registry-based research.
Clinical Research Coordinator II - Clinical Trials Cedars-Sinai Medical CenterClinical Research Coordinator II - Clinical TrialsLos Angeles, CAThe 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. Candidates should also have experience coordinating clinical trials across multiple electronic data capture (EDC) systems and be comfortable managing study data, documentation, and timelines with accuracy and attention to detail.
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 Coordinator I -Surgery Chair Cedars-Sinai Medical CenterClinical Research Coordinator I -Surgery ChairLos 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. 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.
Clinical Research Coordinator I - Guerin Children's - Pediatric Behavioral Neurology - Full-Time, On-Site, Days Cedars-Sinai Medical CenterClinical Research Coordinator I - Guerin Children's - Pediatric Behavioral Neurology - Full-Time, On-Site, DaysLos 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. 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.
Clinical Research Financial Analyst Children's Hospital Los AngelesClinical Research Financial AnalystLos Angeles, CA$71,760–$87,360 / yearPurpose Statement/Position Summary: Under limited direction, the Clinical Research Financial Analyst will be responsible for one or more aspects of the financial management of the clinical trials of The Saban Research Institutes (TSRI). Children's Hospital Los Angeles is consistently ranked among the top 10 children s hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.
NewClinical Research Coordinator I - Karsh Division of Gastroenterology and Hepatology Cedars-Sinai Medical CenterClinical Research Coordinator I - Karsh Division of Gastroenterology and HepatologyLos Angeles, CAThe Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The Karsh Division of Gastroenterology and Hepatology offers trusted care from doctors and researchers who have pioneered many of the diagnostic techniques and surgical treatments widely used to treat digestive and liver diseases.
Clinical Research Associate | Remote Sonova Holding AGClinical Research Associate | RemoteValencia, CARemote$72,000–$90,000 / yearPreferred qualifications include: a Masters degree or equivalent; ACRP-CRA, ACRP-CP, or SOCRA CCRP certification; experience with Class III medical device clinical trials, global multicenter studies, FDA IDE/PMA or EU MDR clinical studies; and knowledge of Risk-Based Monitoring/RbQM. In this role, you will work closely with investigative sites and cross-functional teams to support high-quality clinical research, maintain regulatory compliance, and contribute to studies that support innovative hearing healthcare technologies.
Clinical Research Data Specialist I - Ouyang Lab Cedars-Sinai Medical CenterClinical Research Data Specialist I - Ouyang LabLos Angeles, CAHis previous work has demonstrated the ability of convolutional neural networks to identify systemic human phenotypes that modify cardiovascular risk previously thought to be not apparent on echocardiographic images and precision phenotyping of cardiac function with higher precision than human interpreters. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research.
Clinical Research Data Specialist I Cedars-Sinai Medical CenterClinical Research Data Specialist ILos Angeles, CA$24–$39.76 / hourCountry Code+1+1242+1246+1264+1268+1284+1340+1441+1473+1649+1664+1670+1671+1684+1758+1767+1784+1849+1868+1869+1876+1939+20+211+212+213+216+218+220+221+222+223+224+225+226+227+228+229+230+231+232+233+234+235+236+237+238+239+240+241+242+243+244+245+248+249+250+251+252+253+254+255+256+257+258+261+262+264+265+266+267+268+269+27+290+291+297+298+299+30+31+32+33+34+345+350+351+352+353+354+355+356+357+358+359+36+370+371+372+373+374+375+376+377+378+379+380+381+382+385+386+387+389+39+40+41+420+421+423+43+44+45+46+47+48+49+500+501+502+503+504+505+506+507+508+509+51+52+53+54+55+56+57+58+590+591+593+594+595+596+597+598+599+60+61+62+63+64+65+66+670+672+673+674+675+676+677+678+679+680+681+682+683+685+686+687+688+689+690+692+7+77+81+82+84+850+852+853+855+856+86+872+880+886+90+91+92+93+94+95+960+961+962+963+964+965+966+967+968+970+971+972+973+974+975+976+977+98+992+993+994+995+996+998Phone Number. Req ID 16722 Working Title Clinical Research Data Specialist I Department Research - Hematology and Cellular Therapy 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 $24.00 - $39.76.