NewRadiation Therapist - Radiology Oncology Providence Health and ServicesRadiation Therapist - Radiology OncologySanta Rosa, CA$58.07–$90.14 / hour10,000 Sign-on Bonus for eligible rehire and external candidates who meet all conditions for payment - this is in addition to the fantastic benefits and compensation package offered by Providence that begin on your first day of employment. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington.
Director, Biostatistics - Remote Agios PharmaceuticalsDirector, Biostatistics - RemoteSan Francisco, CARemote$183,000–$275,000 / yearThe current base salary range for this position is expected to be between $183,000 and $275,000 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. The Director will serve as the lead statistician for assigned clinical development programs, leading the development and implementation of statistical solutions to support all phases of clinical trials, regulatory filing and facilitating decision-making.
Travel Speech Language Pathologist (SLP) in Oakland, CA AlliedTravelCareersTravel Speech Language Pathologist (SLP) in Oakland, CAOakland, CASource=AYA;SourceID=3341930; Status=Open;Association=Vaya MSP; Client=UCSF Health Benioff Children's Hospital - Oakland; City=Oakland; State=CA; Zip=94609; Start=8/3/2026;End=12/7/2026;Duration=126;Cert=Therapy/Rehabilitation; Specialty=SLP Pediatrics; Unit=7780500 - Speech Therapy; Shift=Day 5x8-Hour (08:00 - 16:30);# of Postions=1;Type=Travel;BillRate=108.00;OTRules=8 regular hours in a day AND 40 regular hours in 1 week: 1.3%; Orientation=24; Description=Oakland 8 HR Days (M-F) Required: CCC-SLP BLS Min 2 Years Exp (Min 1 year of hospital exp) Acute care Exp. RTO cannot be within the first two weeks of start _x000D_ _x000D_ Locals: _x000D_ Accepted and have the same rates as Travel _x000D_ _x000D_ Charting: _x000D_ Epic; refer to UD on whether required or preferred _x000D_ _x000D_ Certs: _x000D_ BSN required for all RN positions; CA license in hand required for all RN positions _x000D_ _x000D_ Return Staff: _x000D_ ANY employment with any University of California medical facility and any of their acquired facilities MUST be included with employment history.
Clinical Trial Manager/Sr Clinical Trial Manager ErascaClinical Trial Manager/Sr Clinical Trial ManagerSouth San Francisco, CAThe position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Our programs take novel approaches to shutting down one of cancer's most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide.
Clinical Trial Manager/Sr Clinical Trial Manager Erasca IncClinical Trial Manager/Sr Clinical Trial ManagerSan Diego, CA$145,000–$190,000 / yearThe position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out, including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Essential Duties and Responsibilities: Manage global clinical trials (Phase 1-3) in oncology indications, ensuring that studies are carried out in accordance with the clinical development plan, ICH-GCP, and FDA/other regulatory agency requirements.
Senior Clinical Trial Manager Natera IncSenior Clinical Trial ManagerCA$131,900–$164,900 / yearThe Clinical Trial Manager should have experience in managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
Senior Clinical Trial Manager - Oncology - U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Trial Manager - Oncology - U.S. (Remote)CARemote$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.
Clinical Trial Manager National InstituteClinical Trial ManagerHuntington Beach, CaliforniaPerform or provide direct oversight of Clinical Research Coordinator responsibilities, including subject visits, informed consent, source documentation, investigational product accountability, data entry, query resolution, scheduling, specimen processing, and sponsor communication when necessary to support site operations. Additionally, you will formally supervise, support, and mentor clinical staff—including Coordinators, Principal Investigators, and Sub-Investigators—to optimize patient flow and deliver exceptional performance.
Clinical Trial Manager Imperative Care IncClinical Trial ManagerCampbell, CA$136,000–$152,000 / yearAs a seasoned Clinical Trials Manager, this role will carry out all tactical aspects of assigned clinical trials from study initiation to monitoring adherence to design protocols, identifying and resolving issues at study sites and with CROs, and facilitating effective clinical programs. Imperative Care considers factors such as scope and responsibilities of the position, candidates work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.
Clinical Trial Manager Imperative CareClinical Trial ManagerCampbell, CAFull timeImperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. Contribute operational expertise to the development of study protocols, clinical study documents, and cross-functional clinical initiatives that support innovative neurovascular medical device programs.
Clinical Trial Manager Sagimet Biosciences IncClinical Trial ManagerSan Mateo, CA$90–$135 / hourAdditional responsibilities include Independent oversight of outsourced clinical studies, protocol review for operational feasibility and consistency, CRO/vendor feasibility, request for proposal and bid defense process, country/site feasibility, tracking site selection, activation, and patient recruitment. Work with junior CTM for oversight of Trial Master Files (TMF) oversight plan and laisses with CRO for annual quality check; ensuring tracking of ICH-GCP and/or FDA CRF21 essential study documents.
Clinical Trial Manager CareDx IncClinical Trial ManagerBrisbane, CARemote$124,000–$155,000 / yearSpecific responsibilities include, but are not limited to: Lead the end-to-end execution of CareDx clinical trials, including but limited to site identification, study start-up, study conduct, monitoring and closeout, with full accountability of study timelines, budget and metrics; study submission to IRB/ECs; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab test requisitions, etc.), plans and managing study-specific meetings (e.g. Provide cross-functional leadership across Clinical Operations, Data Management, Medical Affairs and other functional areas serving as the central point of coordination to ensure clear roles, accountability, and seamless clinical trial execution.
Clinical Trial Manager Ossium Health IncClinical Trial ManagerSan Francisco, CA$145,000–$165,000 / yearThis position is ideal for someone who thrives in a hands-on, fast-paced environment-someone eager to collaborate across teams and coordinate with internal partners, CROs, and external vendors to deliver excellence in every aspect of our trials. Review and contribute clinical operations input to key study documents including protocols, investigator brochures, regulatory submissions, clinical study reports, and operational plans developed by CRO partners.
Clinical Trial Manager Ossium HealthClinical Trial ManagerSan Francisco, CaliforniaThis position is ideal for someone who thrives in a hands-on, fast-paced environment—someone eager to collaborate across teams and coordinate with internal partners, CROs, and external vendors to deliver excellence in every aspect of our trials. Review and contribute clinical operations input to key study documents including protocols, investigator brochures, regulatory submissions, clinical study reports, and operational plans developed by CRO partners.
Clinical Trials Manager (Biotechnology, Oncology) Exelixis IncClinical Trials Manager (Biotechnology, Oncology)Alameda, CA$136,000–$192,500 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BA/BSN in biological sciences or related field and a minimum of 7 years of related experience; or, MS/MA/MSN in biological sciences or related field and a minimum of 5 years of related experience; or, PhD/PharmD in biological sciences or related field and zero or more years of related experience; or, Equivalent combination of education and experience. This position is responsible for overseeing the execution of clinical trials, collaborating with cross-functional teams, performing oversight activities of Contract Research Organizations (CROs), and providing operational support to the Study Delivery Lead (SDL).
Sr. Clinical Trials Manager - VahatiCor T45 LabsSr. Clinical Trials Manager - VahatiCorSanta Clara, CaliforniaRemoteDemonstrated experience leading study-level clinical operations activities, including study startup, vendor management, enrollment forecasting, study metrics, and cross-functional execution. This role serves as the study-level operational owner, accountable for timelines, budgets, vendor performance, enrollment forecasting, study metrics, risk management, and cross-functional execution.
Clinical Trial Manager CTM Corcept Therapeutics IncClinical Trial Manager CTMRedwood City, CA$156,600–$184,300 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Manages, either directly or through supervised delegation, other study-wide activities such as external vendors, sample handling, drug re-supply, investigator payments, overall data quality, and overall central records quality.
Clinical Trial Manager University of California, IrvineClinical Trial ManagerIrvine, CaliforniaFull timeThe Susan Samueli Integrative Health Institute (SSIHI), part of UCI Health and the Susan & Henry College of Health Sciences, works to transform healthcare through the practice of integrative health by conducting rigorous research, promoting evidence-based treatment modalities, educating the public on well-being practices, providing individualized, patient-centered clinical care, and providing services to the community that focus on obtaining optimal health. Responsibilities: The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high-quality clinical research programs across the Susan Samueli Integrative Health Institute (SSIHI), while strategically guiding industry sponsors, faculty, and research teams, through successful partnerships with the University of California, Irvine (UCI).
Senior Clinical Trials Manager (Biotech Oncology) Exelixis IncSenior Clinical Trials Manager (Biotech Oncology)Alameda, CA$172,000–$245,000 / yearApproaches problems and solutions with an enterprise mindset, considering broad impact to portfolio, regional, and global functions • Ability to study, analyze, and understand new situations and business problems and identify appropriate solutions • Curious in planning; agile in execution • Operationally excellent and drives others towards excellence • Resilient in the context of a rapidly changing environment • Organized with a systematic approach to prioritization. Education/Experience: • BA/BS in biological sciences or related field and a minimum of 9 years of related experience; or, • MA/MS in biological sciences or related field and a minimum of 7 years of related experience; or, • PhD/PharmD in biological sciences or related field and a minimum of 2 years of related experience; or, • Equivalent combination of education and experience.
Senior Clinical Trial Manager Sr CTM Corcept Therapeutics IncSenior Clinical Trial Manager Sr CTMRedwood City, CA$170,500–$200,700 / yearThis leader will work with cross-functional teams as well as vendors, clinical sites, and CROs to execute protocol requirements to ensure study deliverables, milestones, and objectives are met within timelines and budget. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Clinical Trial Manager Braveheart BioClinical Trial ManagerSan Francisco, CaliforniaPerform accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure study procedure conduct is in accordance with SOPs and protocol procedures and review routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required. Our lead product candidate, BHB-1893, is a next-generation oral small-molecule cardiac myosin inhibitor (CMI) being developed for the treatment of obstructive HCM (oHCM) and non-obstructive HCM (nHCM).
Clinical Trial Manager Thorough GroupClinical Trial ManagerSan Diego, CaliforniaThis individual will play a critical role in study start-up, site activation, enrollment strategy, risk management, and overall trial execution while collaborating closely with cross-functional stakeholders across the organization. As the organization continues to advance its pipeline, they are seeking an experienced and highly motivated Clinical Trial Manager (CTM) to provide operational leadership for ongoing and upcoming clinical studies.
SR. CLINICAL TRIAL MANAGER Sutro Biopharma IncSR. CLINICAL TRIAL MANAGERSouth San Francisco, CA$155,000–$175,000 / yearSutro is advancing a robust early-stage pipeline of novel exatecan and dual-payload antibody drug conjugates (ADCs), coupled with high-value collaborations and industry partnerships, which validate its continuous product innovation. 7+ years of experience with 5+ or more years of experience in clinical operations, study coordinator, data management, site monitoring and/or nursing experience preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate's eligibility.
Sr. Clinical Trial Manager Structure Therapeutics IncSr. Clinical Trial ManagerSouth San Francisco, CA$171,000–$218,000 / yearManages study sites and study-related activities, including but not limited to: • Site feasibility selection • Start-up • Subject recruitment • Enrollment • Study management • Monitoring • Report review • Site management • Trial master files • Data review • Clean-up • Coordinates with Lead and Finance to track the financial status against budget. • In collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers budgets and proposals, conduct bid defense meetings, award services, negotiate, and execute complex agreements (e.g., CRO study-related collaboration agreements).
Clinical Trial Manager Structure Therapeutics IncClinical Trial ManagerSouth San Francisco, CA$146,000–$185,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers budgets and proposals, conduct bid defense meetings, award services, negotiate, and execute complex agreements (e.g., CRO study-related collaboration agreements). The companys platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Clinical Trial Manager, Oncology, Asia Eikon Therapeutics IncClinical Trial Manager, Oncology, AsiaMillbrae, CA$130,000–$142,500 / yearCollaborate with other Clinical Operations functions (Site Engagement & Monitoring Excellence) to efficiently and effectively deliver study site initiation, training, and monitoring activities to ensure adherence to study protocols, regulatory requirements, and ICH-GCP guidelines. In partnership with Clinical Study Management, provide guidance and daily oversight for the successful in-house management of all aspects of international in-sourced clinical trials, delivering high quality study data, on time and on budget.
NewCancer Clinical Trial Budgets Finance Manager (Hybrid) Stanford UniversityCancer Clinical Trial Budgets Finance Manager (Hybrid)Stanford, CAThe Stanford University NCI Designated Cancer Clinical Trials Office seeks a Research Administrator 4 to lead and manage a budget finance team responsible for clinical trial budget preparation, negotiation and proposal submission for a large volume of diverse and complex, sponsored clinical research, involving multiple sub-sites, sub-awards, principal investigators, and/or cross-department initiatives. This includes protocol review and interpretation, interpretation and application of pertinent government regulations and guidelines, develops budgets, negotiates and provides strategic advice to the PI, ensuring that the contract budgets and payment schedules/terms meets sponsor, University, hospital and School pre-and post- award guidelines/regulations.
Manager, Clinical Trial Managers - CNS - U.S. (Remote) Worldwide Clinical Trials Holdings IncManager, Clinical Trial Managers - CNS - U.S. (Remote)CARemote$112,000–$222,000 / yearThe Manager, Clinical Operations Site Management (Franchise Lead) is responsible for providing on‑time and quality delivery of site management services from assigned Clinical Trial Managers (CTMs) within assigned therapeutic area(s) and program(s). Establish regular communication to include quality metrics (such as site visit report compliance, source data verification metrics, and on‑site metrics) and overall project "health" metrics (such as data query status, adherence to the scope of work, and resource status).
Senior Manager, Clinical Trials Kaiser PermanenteSenior Manager, Clinical TrialsLos Angeles, CACoordinates and manages clinical research by: providing guidance across teams and in research proposal preparation and submission for portfolios of various trials as applicable; manages multiple teams in the collection, management, analyses, and interpretation of clinical trials data; orchestrating internal resources needed to provide consultation on implementing clinical trials for staff; driving the development and implementation of policies and procedures for developing research protocols and other processes of clinical trials; reviewing, editing, and ensuring accurate compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for overseeing and managing 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 overseeing 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). + Guides research compliance by: leveraging advanced knowledge of clinical trials while influencing the development and implementation of organizational policies and protocols for clinical trial applications in compliance with all applicable federal, state, and local regulations; resolving escalations of compliance and/or quality issues and providing oversight for corrective action plans; disseminating compliance requirement updates to precipitate necessary updates for compliance-monitoring/audit systems and documentation; monitoring and ensuring adherence to new or updated research protocols, procedures, and guidance to continuously improve the confidentiality, privacy, and security of clinical research data; planning the implementation of research protocols, procedures and guidance to ensure confidentiality, privacy, and security of clinical research data within and across units; and overseeing, advising, and providing strategic direction to investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines.
Principal Product Manager, Clinical Trials Intelligence Revolution Medicines IncPrincipal Product Manager, Clinical Trials IntelligenceRedwood City, CA$211,000–$264,000 / yearRequired Skills, Experience and Education: 12+ years of experience in Product Management, Clinical Data Product Management, Clinical Informatics, Clinical Operations Technology, Clinical Systems, Digital Health, Life Sciences Data Platforms, or related roles within biotech, pharma, CRO, healthcare technology, or another regulated environment. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Principal Product Manager, Clinical Trials Intelligence Revolution MedicinesPrincipal Product Manager, Clinical Trials IntelligenceRedwood City, CaliforniaThe company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. 12+ years of experience in Product Management, Clinical Data Product Management, Clinical Informatics, Clinical Operations Technology, Clinical Systems, Digital Health, Life Sciences Data Platforms, or related roles within biotech, pharma, CRO, healthcare technology, or another regulated environment.
NewClinical Trial Manager University of CaliforniaClinical Trial ManagerIrvine, CA2025 University of California, Irvine, UCI Health, and UC Regents. Sign-up to be notified of hiring events, newly posted job opportunities, and much more.
Senior Manager, Clinical Trials Sonova Holding AGSenior Manager, Clinical TrialsValencia, CA$131,560–$164,450 / yearBuild and lead a high-performing team of data managers and scientists; establish data management capabilities, drive evidence generation to support product registration and clinical claims, and lead the build-out of Global Clinical Trials infrastructure including SOPs, systems, governance, and continuous improvement. Proven ability to build strong relationships with external partners, CROs, and vendors; demonstrated experience managing contracts and clinical finance activities across global studies; strong track record in timeline and budget management for complex, multi-country clinical trials.
Associate Clinical Trial Manager Erasca IncAssociate Clinical Trial ManagerSan Diego, CA$122,000–$137,000 / yearThe position requires knowledge of clinical trial processes and experience in many aspects of trial execution from study start-up to close-out, including assisting in the management of clinical vendors or CROs and assisting in the oversight of resources, budgets, contracts, and timelines. Clinical Project Manager of Clinical Operations, the Associate Clinical Trial Manager (aCTM) will assist in the implementation and conduct of clinical research projects and provide support for project teams.
Clinical Trial Manager, CKD Maze Therapeutics IncClinical Trial Manager, CKDSouth San Francisco, CA$143,000–$175,000 / yearOur clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. Steer the execution of one or more of our Phase 2 CKD clinical trials; from protocol development to achievement of corporate and study milestones such as first patient in, interim analysis, database lock, and study report completion.
Subject Mater Expert, Clinical Trials HCTHealthcareSubject Mater Expert, Clinical TrialsSan Jose, CAKeywords: Subject Matter Expert (SME), Clinical Trial Subject Matter Expert, Clinical Research Consultant, Clinical Research Manager, Clinical Trial Manager (CTM), Senior Clinical Trial Manager, Clinical Operations Manager, Director of Clinical Operations, Associate Director of Clinical Operations, Clinical Program Manager, Clinical Project Manager, Clinical Development Manager, Clinical Research Scientist, Clinical Scientist, Medical Affairs Manager, Research Nurse, Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Principal CRA, Clinical Trial Lead, Clinical Trials, Clinical Research, Clinical Operations, Phase I, Phase II, Phase III, Phase IV, Investigator-Initiated Trials (IIT), Multicenter Studies, Global Clinical Trials, Site Management, Trial Startup, Study Start-Up, Patient Recruitment, Site Activation, Clinical Monitoring. Experience: Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelor’s degree may be substituted for one (1) year work experience).
Clinical Trial Assistant Sagimet Biosciences IncClinical Trial AssistantFoster City, CAThe CTA will play a hands-on role in trial start-up, maintenance, and close-out activities, partnering closely with Clinical Trial Managers (CTMs),, vendors, and cross-functional internal stakeholders. The Clinical Trial Assistant (CTA) provides operational and administrative support to the Clinical Operations team in the execution of Sagimet's clinical trials.
Lab Tech I - Research Assistant (Clinical Trials) Collaborative Neuroscience Research, LLCLab Tech I - Research Assistant (Clinical Trials)Garden Grove, CA$20–$21.50 / hourPart timeWe focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Clinical Trial Management Associate, Oncology EMEA/LATAM Eikon Therapeutics IncClinical Trial Management Associate, Oncology EMEA/LATAMMillbrae, CA$122,000–$133,000 / yearEikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. You are looking to grow beyond a CTA role and take on more direct responsibility for study deliverables, bringing with you valuable clinical research experience and a strong passion to contribute meaningfully to drug development through consistent operational excellence.
Sr. Clinical Trials Associate II HonorVet TechnologiesSr. Clinical Trials Associate IIAliso Viejo, CA$62.64–$78.34 / hourWith strong delivery capabilities and rapid turnaround times, we support contract, direct hire, project-based, and consulting staffing needs across clinical research, pharmacovigilance, regulatory affairs, quality assurance, quality control, medical affairs, manufacturing, validation, and scientific operations. HonorVet Technologies (SDVOSB) provides specialized and scalable staffing solutions to pharmaceutical companies, medical device companies, biotech organizations, CROs, research laboratories, and life sciences organizations across the United States.
Clinical Trials Associate II Glaukos CorpClinical Trials Associate IIAliso Viejo, CAOur constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Licensed Vocational Nurse - Clinical Trials (Nights) Collaborative Neuroscience Research, LLCLicensed Vocational Nurse - Clinical Trials (Nights)Los Alamitos, CA$32–$34 / hourPart timeProvides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Sr. Clinical Trials Associate - Onsite in Aliso Viejo, CA Glaukos CorpSr. Clinical Trials Associate - Onsite in Aliso Viejo, CAAliso Viejo, CAOur constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
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.
Sr. Clinical Trials Associate II Glaukos CorpSr. Clinical Trials Associate IIAliso Viejo, CAClinical site and vendor management: oversee communication with clinical sites and vendors, managing site activities such as initiation, monitoring, and close-out visits, and proactively resolving site-related issues. Cross-functional leadership: act as a liaison with Clinical Operations, CMC, Finance, Business Systems, and research teams, aligning project objectives and supporting efficient, high-quality study operations.
Research Nurse IV, LPN / LVN, Clinical Trials Kaiser PermanenteResearch Nurse IV, LPN / LVN, Clinical TrialsLancaster, 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.
Lab Tech I - Research Assistant (Clinical Trials) CenExelLab Tech I - Research Assistant (Clinical Trials)Garden Grove, CaliforniaWe focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Associate Clinical Trials Administrator Procept Biorobotics CorpAssociate Clinical Trials AdministratorSan Jose, CA$82,110–$96,600 / yearIt continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept's history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.
Licensed Vocational Nurse - Clinical Trials (Nights) CenExelLicensed Vocational Nurse - Clinical Trials (Nights)Los Alamitos, CaliforniaProvides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Manager, Clinical Programs ImmunityBio IncManager, Clinical ProgramsEl Segundo, CACompany Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patients natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. Knowledge, Skills, & Abilities • Strong background in oncology clinical development • Demonstrated ability working directly with the highest levels of the company with ease • Excellent verbal and written communication skills in English • Knowledge of FDA guidelines as well as ICH/GCP Guidelines.