Regional Clinical Study Associate Manager BeOne Medicines AGRegional Clinical Study Associate ManagerCA$96,300–$131,300 / yearManages the regional clinical operations team (incl oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study, or supports the Regional Clinical Study (Sr) Manager with specific aspects of regional study delivery. Manages the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study or drives specific aspects of regional study delivery in collaboration with the Regional Clinical Study (Sr) Manager.
Clinical Research Coordinator University of CaliforniaClinical Research CoordinatorLos Angeles, CA$36.37–$58.52 / hourUnder direction of the Principal Investigator (PI) and the CTU/CRS Manager, the employee is to perform research activities directly related to HIV clinical trials in the Center for Clinical AIDS Research and Education (CARE Center) including but not limited to the AIDS Clinical Trials Group (ACTG), HIV Prevention Trials Network (HPTN), HIV Vaccine Trials Network (HVTN), and COVID19 Prevention Trials Network (CoVPN). The incumbent will be directly responsible for assisting with fast-paced implementation of HIV trials; assigned start up and closure of clinical research studies, participant registration, randomization, compliance, participant recruitment, enrollment, data management and education as related to each protocol.
Clinical Research Nurse / Intermittent Hours Parexel International CorpClinical Research Nurse / Intermittent HoursGlendale, CA$40–$47 / hourPerform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation. In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.
Senior Clinical Site Budget Specialist ImmunityBio IncSenior Clinical Site Budget SpecialistEl Segundo, CAGuide and support clinical operations departments in the site budgeting process for ImmunityBio trials, as well as investigator initiated trialsincluding the preparation, negotiation and execution of clinical trial budgets, service contracts and agreements. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response.
Clinical Trials Site Director - Multiple Locations Nationwide Headlands Research IncClinical Trials Site Director - Multiple Locations NationwideCAThis general interest posting is designed for Site Directors who may not see a current opening that aligns with their location-but who would like to be considered for future leadership opportunities across our growing network of clinical research sites nationwide. Our Site Directors play a critical role in driving site performance, leading cross-functional teams, and ensuring the successful execution of clinical trials in a compliant, patient-centered environment.
Director - Clinical Research Billing (Remote - CA) Stanford Health CareDirector - Clinical Research Billing (Remote - CA)CARemote$94.35–$125.03 / hourThe Director of Clinical Research Billing will collaborate and have direct interaction with a broad set of stakeholders across the institution, including Principal Investigators, study sponsors, study teams, finance/accounting, revenue cycle, internal audit, compliance, business office leaders, and clinic operational teams. Responsible for overseeing revenue cycle post-award activities, such as research charge review, patient care billing for all clinical trials, reviewing trends in revenue capture and reimbursement, and forecasting financial impacts pertaining to clinical research activities.
Clinical Research Coordinator - Pathology University of CaliforniaClinical Research Coordinator - PathologyLos Angeles, CA$38.19–$61.45 / hourAs a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer. new study/service requests, coordination of specimen handling (procurement, processing, storage, shipping, and distribution).
NewMobile Clinical Research Nurse - Chatsworth, CA Vita MobileMobile Clinical Research Nurse - Chatsworth, CAChatsworth, CAVitaMobile Medical Support Services has an urgent need for a per diem Registered Nurse to join our Clinical Research Team as a Mobile Clinical Research Nurse. Study visit activities include, but are not limited to: Scheduling visits with study participants.
Clinical Research Associate I - Heart Institute - Berman Lab Cedars-Sinai Medical CenterClinical Research Associate I - Heart Institute - Berman LabBeverly Hills, CAFrom 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. The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care.
Senior Director, Global Clinical Data Management ImmunityBio IncSenior Director, Global Clinical Data ManagementEl Segundo, CAImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
Clinical Research Coordinator II - California Heart Center Cedars-Sinai Medical CenterClinical Research Coordinator II - California Heart CenterBeverly Hills, CAPrimary Duties and Responsibilities: Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures, and labs, and completion and maintenance of consent forms, case report forms, SAE's, and source documents.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedCA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Lab Scientist II - Pain Management Quest Diagnostics IncClinical Lab Scientist II - Pain ManagementWest Hills, CA$43.25–$62.10 / hourQuest believes that conviction records may have a direct, adverse, and negative relationship to the following job duties: accessing company property, information, assets, and products including sensitive information; accessing customer data or confidential information, and partnering and regularly working with or supervising other Quest employees and interacting with Quest customers. This may include but not be limited to: evaluation of new techniques and procedures in terms of personnel and requirements, method comparison, cost analysis, establishment of reference ranges, writing and revising technical procedures, and evaluation of productivity and key results measures.
Clinical Research Coordinator II - Medical Group Cedars-Sinai Medical CenterClinical Research Coordinator II - Medical GroupBeverly Hills, CAPrimary Duties and Responsibilities: Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all applicable regulatory requirements.
Clinical Research Associate I - Pulmonary Research Program/Lung Institute Cedars-Sinai Medical CenterClinical Research Associate I - Pulmonary Research Program/Lung InstituteBeverly Hills, CAThe Clinical Research Associate I will work under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. The incumbent will support objectives of research studies through noncomplex tasks such as data collection, prescreening of and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.
Assistant Clinical Research Coordinator - Pediatrics University of CaliforniaAssistant Clinical Research Coordinator - PediatricsLos Angeles, CA$30.74–$49.46 / hourHSR faculty conduct research with systems-level impact on child health in areas including childhood adversity, children with medical complexity, early childhood development, education and school systems, housing and health, obesity prevention, poverty, primary care and healthcare systems, vaccine delivery and uptake, and youth incarceration. The AMP ACEs project is a community-based research initiative designed to evaluate whether a telephone-based Adverse Childhood Experiences (ACEs) screening and care coordination model delivered through 211LA increases referrals to, and receipt of, ACEs-related services.
Clinical Trial Liaison, Director - West AstraZeneca PlcClinical Trial Liaison, Director - WestCA$211,111.20–$316,666.80 / yearThe role is accountable for recommending priority site selection, and setting up a clear field plans consistent engagement expectations across US strategic research centers increasing the consistency, impact, and speed of site-facing medical support for new and ongoing clinical studies across AstraZeneca marketed products, new indications, and compounds in development, including priorities across Cardiovascular, Renal and Metabolic; Respiratory, Immunology; and Vaccines and Infectious Disease. The Regional Director, Clinical Trial Liaison Team will lead and manage a field-based Clinical Trial Liaison team responsible for strengthening scientific engagement with strategic clinical research sites, improving investigator understanding of AstraZeneca trials and pipeline, and helping reduce practical barriers to study start-up, screening, enrollment, referral, and retention.
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.
Clinical Country Site Lead (Southwest) Biogen IncClinical Country Site Lead (Southwest)CA$134,000–$179,000 / yearWorking within Biogen's Internalized Flexible Model, the CCSL partners closely with Clinical Site Engagement and Clinical Monitoring Operations teams, including Clinical Monitoring Leads (CMLs), Site Managers, and FSP partners, to promote seamless collaboration and drive successful country-level study execution. Acting as a key liaison between investigators, research sites, CROs, affiliate teams, and global study teams, the CCSL helps ensure the successful delivery of clinical trials while maintaining a strong focus on quality, patient safety, and operational excellence.
Director, Clinical Affairs Saluda Medical Pty LtdDirector, Clinical AffairsCAWhat Youll Do: Development, maintenance, and optimization of the clinical quality system, clinical regulatory requirements, and data integrity/quality Establish detailed program plans, drive program execution toward established objectives, assess risk and implement strategies to ensure successful delivery of the clinical objectives Contribute to the overall strategic direction for development and implementation of clinical affairs objectives and processes Direct and collaborate with internal and external staff to assure successful conduct of assigned clinical programs consistent with company objectives and applicable regulations and policies Development of protocols, statistical analysis plans, reports and other clinical study documentation Support and contribute to manuscripts, abstracts, data presentations, and health economic value initiatives Promote and embody culture and behavior expectations of a high-performance culture Drives leadership of issue identification and resolution. Knowledge/Skills/Abilities: Excellent verbal and written communication Ability to think creatively, dynamically, and foster a culture of commitment to thoughtful science to help patients in need Knowledge of ICH/GCP and FDA medical device regulations Knowledge of electronic data capture systems and web-based clinical trial management tools Knowledge of research design, data analysis and biostatistics Self-motivated and independent work style with the ability to initiate and follow through on assignments Self-assured, knowledgeable professional capable of developing good interpersonal relationships with medical professionals Excellent organizational skills and attention to detail High degree of personal integrity.