RN Clinical Research -PRN Professional Case ManagementRN Clinical Research -PRNVista, WA$60 / hourWe are looking for CMRNs to visit an Adult population who can perform the following skills during a mobile visit: Blood specimen collection and processing (nurse will pick up dry ice prior to the visit and drop off at UPS after the visit). Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred).
NewClinical Research RN - Research Projects Providence Health and ServicesClinical Research RN - Research ProjectsYorba Linda, CA$54.05–$83.90 / hourSee Providence Health and Services Terms & Conditions at https://www.providence.org/utility-pages/privacy-policy#terms-of-use and Privacy Policy at https://www.providence.org/utility-pages/privacy-policy#privacy-policy and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions. 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.
Clinical Trial Manager/Senior Clinical Trial Manager Janux Therapeutics IncClinical Trial Manager/Senior Clinical Trial ManagerSan Diego, CA$140,000–$154,000 / yearThis individual will be instrumental in managing and overseeing CROs, study vendors, and clinical trial sites, while partnering with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in accordance with regulatory requirements, GCP guidelines, and internal SOPs. In addition to a competitive base salary ranging from $140,000 to $154,000 for Clinical Trial Manager and $160,000 to $178,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus.
Physician, Pediatric Endocrinology (Sacramento, CA) Sutter HealthPhysician, Pediatric Endocrinology (Sacramento, CA)Sacramento, CASMG contains primary care and specialty Physicians and Advanced Practice Clinicians -- nurse practitioners, physician assistants, certified nurse midwives, licensed clinical social workers and licensed marriage and family therapists, who make up about 20% of our group. Just a short drive away, you can find yourself in the bustling city of San Francisco, enjoying the world-class wine country of Napa Valley, or experiencing the stunning natural beauty of Lake Tahoe, which offers both winter sports and summer recreational activities.
Clinical Trial Manager/Senior Clinical Trial Manager Janux TherapeuticsClinical Trial Manager/Senior Clinical Trial ManagerSan Diego, California140,000 - $178,000 a year In addition to a competitive base salary ranging from $140,000 to $154,000 for Clinical Trial Manager and $160,000 to $178,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus. This individual will be instrumental in managing and overseeing CROs, study vendors, and clinical trial sites, while partnering with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in accordance with regulatory requirements, GCP guidelines, and internal SOPs.
Clinical Trial Manager, Clinical Operations CytomX Therapeutics IncClinical Trial Manager, Clinical OperationsSouth San Francisco, CA$135,000–$165,000 / yearWorks directly with study team and/or vendors on development of study documents, plans and manuals including but not limited to: protocol and amendments, investigator brochure, informed consent form, annual reports, clinical study report, pharmacy manual, laboratory manual and internal data review plan. CytomX has a broad pipeline, which comprises seven therapeutic candidates across multiple treatment modalities including antibody-drug conjugates ("ADCs"), T-cell engaging bispecific antibodies ("TCBs"), and immune modulators such as cytokines and checkpoint inhibitors ("CPIs").
Sr. Clinical Research Associate/Clinical Trial Manager BridgeBio Pharma IncSr. Clinical Research Associate/Clinical Trial ManagerSan Francisco, CA$135,000–$177,000 / yearLead aspects of vendor management for the CRO and other key vendors (IRT, imaging, central and specialty labs, etc.), establishing expectations, ensuring deliverables are met, performance measures are maintained, and escalating as needed; address performance gaps and drive corrective actions to closure. Lead operational management for assigned regions and sites by monitoring performance metrics, identifying and mitigating risks, driving escalations and action-item closure, and representing regional performance in study team and cross-functional discussions.
Senior Clinical Trial Manager, Clinical Operations Iambic TherapeuticsSenior Clinical Trial Manager, Clinical OperationsSan Diego, CaliforniaThe Senior CTM is accountable for vendor oversight, risk management, timeline and budget performance, and cross-functional alignment to ensure studies are delivered efficiently and in compliance with global regulatory requirements, ICH-GCP, and company SOPs. In close partnership with Clinical Development, Regulatory, Biometrics, and external CROs, this role drives high-quality, inspection-ready trial execution within a collaborative, growth-stage biotech environment.
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.
Clinical Trial Manager Enigma SearchClinical Trial ManagerCaliforniaLead or co-lead the execution of one or more Phase 2 clinical trials in CKD, overseeing activities from protocol development through key milestones such as first patient in (FPI), interim analysis, database lock, and clinical study report completion. This role is well-suited for someone who enjoys being deeply involved in trial execution, collaborating across functions, and helping bring innovative therapies to patients.
Clinical Trials Manager Resources Connection IncClinical Trials ManagerSouth San Francisco, CAAs the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial stewardship of clinical programs. We've built a global network of over 2,600 experts across four regions, providing a comprehensive suite of solutions across on-demand talent, next-generation consulting, and outsourced services to support organizations at every stage of their growth journey.
NewSenior Clinical Trials Manager ImmunityBio IncSenior Clinical Trials ManagerEl Segundo, CAImmunityBio 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. 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.
Senior Clinical Trials Manager Zai Lab LtdSenior Clinical Trials ManagerSouth San Francisco, CA$177,000–$229,000 / yearParticipates in developing and finalizing cross-functional activities to ensure delivery of critical clinical trial documents such as informed consent forms (ICFs), protocols, site and country budget templates, EDC, IxRS, central/specialty lab, ECG, imaging, PRO specifications, drug supply, biomarker/sample management plans, TMF, and CSRs.\n Drafts and implements study plans including; vendor oversight, risk, quality, safety, communication, trial monitoring, and TMF.\n Ensures TMF creation and QC completion.\n Minimum of 8 years relevant experience of which 5 years are clinical experience in the pharmaceutical industry, including 3 years in study management or equivalent combination of education, training, and experience.\n Ability to work across several time zones.\n \nPREFERRED:\n\n Prior people management experience.\n Demonstrated ability in clinical study management processes and clinical/drug development.\n
NewClinical Trial Manager / Sr. Manager ALX Oncology Holdings IncClinical Trial Manager / Sr. ManagerSouth San Francisco, CA$140,000–$170,000 / yearCTM will actively participate to help develop and execute the clinical trial strategy in support of the Clinical Development Plan, and to work across departments to ensure that studies are planned and conducted efficiently and with the highest quality. Interact collaboratively with Biometrics, Quality, Regulatory, CMC, Finance, and Clinical teams to ensure operational excellence in clinical trial execution to ensure compliance with GCP and ICH guidelines and financial reporting requirements.
Clinical Trial Manager, Clinical Operations CytomX TherapeuticsClinical Trial Manager, Clinical OperationsEmeryville, CaliforniaWorks directly with study team and/or vendors on development of study documents, plans and manuals including but not limited to: protocol and amendments, investigator brochure, informed consent form, annual reports, clinical study report, pharmacy manual, laboratory manual and internal data review plan. CytomX has a broad pipeline, which comprises seven therapeutic candidates across multiple treatment modalities including antibody-drug conjugates (“ADCs”), T-cell engaging bispecific antibodies (“TCBs”), and immune modulators such as cytokines and checkpoint inhibitors (“CPIs”).
NewClinical Trial Manager UCSF Medical CenterClinical Trial ManagerCalifornia, CA$80–$90 / yearIGHS is structured as an Organized Research Unit (ORU) and control point that oversees a portfolio of $330M in sponsored programs (including $80-90M per year in grants and cooperative agreements expenses), two graduate groups that confer Masters and PhD degrees, and an administrative unit that provides communication, financial management, event planning, staffing support, operations, and program development support to faculty members working in global health across the campus. 30 Leads cross-functional study coordination: serves as the primary liaison across the adult and pediatric cohorts, connecting the relevant R2D2 TB Network teams (Technology, GCP Compliance, Data, Clinical Support), international study sites, and sub-contractors, and ensuring aligned communication and accountability across all parties.20
Clinical Trial Manager Caribou Biosciences, Inc.Clinical Trial ManagerBerkeley, CA$145,000–$165,000 / yearCollaborate effectively with Clinical Development, Data Management, Biostatistics, Regulatory Affairs, Medical Monitoring, Drug Supply, Quality Assurance, Safety, and other cross-functional partners to ensure successful trial execution. We believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases.
(Sr.) Clinical Trial Manager (CTM) - Clinical Operations ADARx Pharmaceuticals Inc(Sr.) Clinical Trial Manager (CTM) - Clinical OperationsSan Diego, CAEnsure the successful execution of clinical trial activities with the study team, clinical CROs and other clinical study providers (e.g., core labs, independent contractors) on time, with pre-approval inspection readiness and on budget. Generate and utilize metric reporting (e.g., CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicate issues to Team Members/Vendors, with escalation as appropriate.
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 CareDxClinical 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.