Clinical Trial Manager/Senior Clinical Trial Manager Janux Therapeutics Inc.Clinical 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.
NewSenior Clinical Research Associate, Early Clinical Development IQVIASenior Clinical Research Associate, Early Clinical DevelopmentCarlsbad, CaliforniaConduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I.
Clinical Informaticist - Health Information Systems - IT-Clinical Rady Children's HospitalClinical Informaticist - Health Information Systems - IT-ClinicalSan Diego, CA$48.03–$66.06 / hourUnderstanding of health care patient administration, clinical and business systems and must have installed a minimum of one computer-based hospital system and actively performed the following: process and workflow analysis, systems/applications analysis, project lifecycle implementation with in-depth experience and training in a minimum of four discreet major projects. Must possess skills and experience in oral and written communications; This is applicable to analysis documentation, project management deliverables and documentation, application/systems specifications, project preparation, risk identification and escalation; Ability to present to a broad spectrum of individuals and groups including senior management, physicians and health care professionals.
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.
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 - QA Associate, Clinical Studies Medvacon Life Sciences, LLCClinical - QA Associate, Clinical StudiesSan Diego, CAFull timeAbility to work effectively under pressure to meet deadlines Physical Requirements: • On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. • Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate – Clinical Supplies v1.0.
Clinical - QA Associate, Clinical Studies Medvacon Life Sciences LLCClinical - QA Associate, Clinical StudiesSan Diego, CAAbility to work effectively under pressure to meet deadlines Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Ability to identify aberrant data and potential quality/compliance concerns escalating to management CSD-JD-QA Associate - Clinical Supplies v1.0.
Senior Clinical Scientist / Clinical Scientist CMR Surgical LtdSenior Clinical Scientist / Clinical ScientistSan Diego, CAOur commitment to our goal of building a world-class medical devices company is underpinned by the ground-breaking innovation of our next generation of surgical robots and a diverse team of talented and supportive individuals. We're looking for an exceptional Clinical Scientist / Senior Clinical Scientist to join our Medical Affairs Team, based in Cambridge, and reporting to our Clinical Research Lead.
(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 Research Manager Headlands Research IncClinical Research ManagerEscondido, CA$100,000–$105,000 / yearLead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers, etc. Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Clinical Research Manager Headlands ResearchClinical Research ManagerEscondido, CA$100,000–$105,000 / yearLead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers, etc. Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
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.
Clinical Research Associate, Sponsor Dedicated IQVIAClinical Research Associate, Sponsor DedicatedCarlsbad, CaliforniaPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Ensure 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.
Clinical Research Manager The Neuron Clinic GpClinical Research ManagerSan Marcos, CAFull timeThe Neuron Clinic is looking for a driven and experienced Research Department Manager to lead and elevate our research initiatives. Coordinate trials and/or supervising the clinical research coordinators and research assistants who support trial activities.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)San Diego, CaliforniaFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Coordinator III, Clinical Trials (Durational with Benefits) Kaiser PermanenteClinical Research Coordinator III, Clinical Trials (Durational with Benefits)San Diego, CACompletes work assignments autonomously by applying up-to-date expertise in subject area to generate creative solutions; ensures all procedures and policies are followed; leverages an understanding of data and resources to support projects or initiatives. Supports and develops materials for the education of research staff and/or participants on protocols, documentation procedures, clinical best practices, or timeliness of submissions, with limited guidance.
Director, Key Account Management – IQVIA Clinical Technology IQVIADirector, Key Account Management – IQVIA Clinical TechnologyCarlsbad, CaliforniaIdentifies, or creates opportunities to introduce relevant IQVIANs or teams who are working in areas of high interest for the client, as part of ‘peer to peer’ engagement (i.e., beyond IQVIA capability presentations, or specific pitches / RFPs). Maintains and further establishes strong professional relationships across the client organization; with a particular focus on e-clinical Technology, proactively but appropriately engages with client teams.
Clinical Research Associate II/ Oncology & Ophthalmology/ West region of the US! Thermo Fisher Scientific IncClinical Research Associate II/ Oncology & Ophthalmology/ West region of the US!San Diego, CA$80,000–$125,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
NewResearch Nurse IV, Clinical Trials LVN Kaiser PermanenteResearch Nurse IV, Clinical Trials LVNSan Diego, 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 Associate, Sponsor Dedicated, IQVIA IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated, IQVIACarlsbad, CA$71,900–$182,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.