Clinical Research Coordinator III - Cardiology Cedars-Sinai Medical CenterClinical Research Coordinator III - CardiologyLos Angeles, CAProvides study coordination for assigned projects, including patient screening and consenting, regulatory reporting, completion required data collection, maintenance of source documents, facilitation of all study logistics to ensure successful protocol implantation and patient safety. This includes managing schedules and coverage for the coordinator team, improving efficiency of research systems and processes, training of personnel, and resolution of day-to-day administrative and operational problems to ensure the successful implementation of research protocols.
Clinical Research Advanced Practice Provider West DermatologyClinical Research Advanced Practice ProviderSanta Ana, California$65–$70 / hourThe Clinical Research Nurse Practitioner/Physician Assistant will work closely with the Principal Investigator to support clinical research studies that specifically focus on diabetes and weight management. The Clinical Research Nurse Practitioner/Physician Assistant will work closely with the Principal Investigator to support various clinical research studies at Southern California Clinical Research.
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.
Senior Clinical Trial Manager - Oncology - U.S. Worldwide Clinical Trials Holdings IncSenior Clinical Trial Manager - Oncology - U.S.CA$112,000–$222,000 / yearClinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
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.
Clinical Research Coordinator The Los Angeles Cancer NetworkClinical Research CoordinatorFountain Valley, California$75,000–$80,000 / yearThe Clinical Research Coordinator 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.
Director, AI Clinical Operations & Regulatory Edwards Lifesciences CorpDirector, AI Clinical Operations & RegulatoryIrvine, CA$202,000–$287,000 / yearWhat you'll need (Required): Bachelor's Degree in related discipline, with 12 years of experience in clinical development operations, data management, biometrics, or regulatory operations, or equivalent leadership at a clinical technology vendor or CRO -OR- Master's, PhD, or other advanced degree with 10 years of experience in clinical development operations, data management, biometrics, or regulatory operations, or equivalent leadership at a clinical technology vendor or CRO. Familiarity with AI-driven patient recruitment and site-selection approaches from biopharma trial operations: NLP-based EHR mining for eligibility screening, digital biomarkers and wearable data for continuous safety monitoring, and in silico trial simulation for protocol feasibility testing.
Clinical Research Associate II Ora IncClinical Research Associate IICAConducts site visits including but not limited to evaluation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Clear and Direct Communication, Feedback and Conflict Resolution: Practice radical candor in your communication and participate in active Giving and receiving feedback frequently, with an open heart and mind creates psychological safety and promotes faster, individual, team and company growth.
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.
Clinical Research Manager Envista DentistryClinical Research ManagerBrea, California$125,500–$153,400 / yearEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
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.
Clinical Positions in Clinical Nutrition 2026-2027 University of California Los AngelesClinical Positions in Clinical Nutrition 2026-2027Los Angeles, CA$146,700–$442,800 / yearThe Division of Clinical Nutrition in the Department of Medicine at the David Geffen School of Medicine at UCLA invites applicants for a faculty position in the Health Sciences Clinical Professor series at the Instructor, Assistant, Associate, or full Professor ranks. The University of California promotes the social mobility of its students, equips them with the tools and experience that furthers their ambitions, and regards their accomplishments across the life span as evidence of the profoundly positive impact of higher education.
Research Compliance Analyst III Tulane UniversityResearch Compliance Analyst IIILa, CAPreferred Qualification: Juris Doctorate or other advanced degree, or a combination of Bachelor's Degree with three to five years of experience working in human subjects research either in the capacity as a researcher or research management. Minimum Qualification: Bachelor's Degree and three (3) years of human subjects clinical research experience, including legal and/or regulatory research experience.
NewSenior Manager, Statistical Programming Edwards Lifesciences CorpSenior Manager, Statistical ProgrammingCA$151,000–$215,000 / yearFrequently interacts with customers, and/or functional peer group managers, normally involving matters between cross-functional teams and the company; often leads a cooperative effort among members of a project team. Lead a team of programmers in collaboration with cross-functional teams to ensure that database and external data source when applicable meet analysis requirements across clinical trials.
Group Product Manager - US Marketing Edwards Lifesciences CorpGroup Product Manager - US MarketingIrvine, CA$145,000–$205,000 / yearHow you'll make an impact: The Group Product Manager, US Marketing will develop and execute an annual product marketing plan, including a variety of marketing/related activities to effectively market Edwards existing products to constituents including physicians, hospital staff, and the Edwards field team (e.g., sales representatives, clinical specialists). Possess strong clinical knowledge, experience and knowledge of the clinical areas where Edwards' products are used or intended to be used, understand the purchasing process and challenges for product adoption in complex healthcare networks.
Regional Medical Scientific Director-Thoracic Malignancies (Los Angeles) Merck & Co IncRegional Medical Scientific Director-Thoracic Malignancies (Los Angeles)Los Angeles, CA$210,400–$331,100 / yearMust possess a thorough understanding of the United States Federal Drug Administration (FDA), Office of Inspector General (OIG), Health Insurance Portability and Accountability Act (HIPAA) and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. The Oncology Regional Medical Scientific Director, RMSD, is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community.
Registered Nurse Clinical II, Telemetry **8K Sign on Bonus** - Full Time Nights Valley Presbyterian HospitalRegistered Nurse Clinical II, Telemetry **8K Sign on Bonus** - Full Time NightsVan Nuys, CAFull timeWe’re seeking an experienced Registered Nurse (Clinical II) to coordinate patient care, support clinical excellence, and contribute to a collaborative healthcare environment. At Valley Presbyterian Hospital, our nurses are essential to delivering safe, compassionate, and efficient care.
Registered Nurse Clinical II, Operating Room **$8K Sign-On Bonus** - Full Time Days Valley Presbyterian HospitalRegistered Nurse Clinical II, Operating Room **$8K Sign-On Bonus** - Full Time DaysVan Nuys, CAFull timeWe’re seeking an experienced Registered Nurse (Clinical II) to coordinate patient care, support clinical excellence, and contribute to a collaborative healthcare environment. At Valley Presbyterian Hospital, our nurses are essential to delivering safe, compassionate, and efficient care.
Registered Nurse/Clinical II, Operating Room Unit **$8K Sign-On Bonus** - Full Time Days Valley Presbyterian HospitalRegistered Nurse/Clinical II, Operating Room Unit **$8K Sign-On Bonus** - Full Time DaysVan Nuys, CAFull timeWe’re seeking an experienced Registered Nurse (Clinical II) to coordinate patient care, support clinical excellence, and contribute to a collaborative healthcare environment. At Valley Presbyterian Hospital, our nurses are essential to delivering safe, compassionate, and efficient care.
Registered Nurse Clinical II, Emergency Room **8K Sign on Bonus** - Full Time Nights Valley Presbyterian HospitalRegistered Nurse Clinical II, Emergency Room **8K Sign on Bonus** - Full Time NightsVan Nuys, CAFull timeWe’re seeking an experienced Registered Nurse (Clinical II) to coordinate patient care, support clinical excellence, and contribute to a collaborative healthcare environment. At Valley Presbyterian Hospital, our nurses are essential to delivering safe, compassionate, and efficient care.