Vendor Management Specialist Project Management Pyramid Consulting, IncVendor Management Specialist Project ManagementFoster City, CA$40–$43 / hourExperience with vendor management, vendor qualification, vendor assessment, supplier management, vendor oversight, CRO management, outsourcing, sourcing, procurement, or external partner management. Key Responsibilities: Lead and/or support vendor qualification and capability assessment activities for external vendors supporting global R&D and clinical development programs.
Clinical Informatics Specialist LatentClinical Informatics SpecialistSan Francisco, CaliforniaThe Clinical Specialist will play a critical role in data generation, annotation, and evaluation to improve Latent’s AI models, while also serving as a clinical subject matter expert (SME) to inform feature development, workflows, and internal tooling. Background in pharmacy practice, including formal training or certification as a Pharmacist or Pharmacy Technician, Physicians Assistant, Nurse Practitioner, Nurse or equivalent hands-on clinical experience.
Medical Science Liaison - Medical Devices LancesoftMedical Science Liaison - Medical DevicesSanta Clara, CA$52MSLs engage in scientific discussions, attend medical conferences, and deliver presentations to ensure that stakeholders are well-informed about the latest research and product developments. Their primary role is to disseminate scientific information, provide clinical and scientific support for products, and gather insights from the field to inform the company's strategic direction.
Life Sciences Associate OsmindLife Sciences AssociateSan Francisco, CA$110,000–$125,000 / yearOur Biosciences team turns that data and clinical footprint into partnerships with biopharma companies across our four life sciences product lines: clinical real-world evidence, clinical research, commercial real-world evidence, and sales & marketing solutions. Leverage your client-facing abilities to develop deep relationships, effectively project manage client projects, and identify and execute on cross-sell and upsell opportunities.
FSP - QC Reviewer: Small Molecule Thermo Fisher ScientificFSP - QC Reviewer: Small MoleculeFoster City, CaliforniaWithin our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Respiratory Therapy Manager – Acute Care Hospital Midland-MarvelRespiratory Therapy Manager – Acute Care HospitalSan Francisco, CA$191,000–$222,000 / yearThe combination of adult acute care, Level III NICU services, clinical innovation, quality improvement, staff development, and operational responsibility makes this an excellent next step for a Respiratory Therapy Manager looking to expand their leadership impact. We are seeking a proven Respiratory Therapy leader with significant inpatient hospital management experience, adult acute care and Level III NICU experience, and recent experience working in a union environment .
Senior Director, Translational Medicine And Clinical Biomarkers Nurix Therapeutics, Inc.Senior Director, Translational Medicine And Clinical BiomarkersBrisbane, CA$280,400–$316,500 / yearD. or MD strongly preferred) with 12+ years of experience in a relevant scientific area within the pharmaceutical or biotech industry, including significant experience in clinical-stage drug development; deep translational biomarker expertise in Immunology, Oncology, or Hematology strongly preferred. Demonstrated track record of developing and leading biomarker strategy across a clinical portfolio - spanning multiple programs or indications - with direct experience influencing clinical trial design and regulatory submissions.
Nurse Manager II, Care at Home (Strong Home Health experience Required) Kaiser PermanenteNurse Manager II, Care at Home (Strong Home Health experience Required)Oakland, CA$239,000–$276,100 / yearManages improvements to operations and technology processes by: leading and implementing long-term strategic projects designed to remediate issues and improve quality, service, affordability, and/or operating efficiency; developing and managing a structured approach for identifying root causes and implementing solutions to improve the performance of operations system processes in response to barriers and/or issues; and ensuring performance metrics used to monitor the success of strategic improvement projects are tied to strategic organizational initiatives. Manages designated units or teams by translating business plans into tactical action items; oversees the completion of work assignments and identifies opportunities for improvement; ensures all policies and procedures are followed; partners with key stakeholders and business leaders to ensure products and/or services meet requirements and expectations while aligning with departmental strategies.
Senior Clinical Practice Nurse II - Magnet Programs Kaiser PermanenteSenior Clinical Practice Nurse II - Magnet ProgramsSan Francisco, CADrives training and education by: providing consultation, designing, and delivering advanced training and educational programs to drive strategic organizational objectives for staff and practitioners; mentoring and coaching staff and stakeholders on complex policies, procedures, protocols, educational programs, and strategic best practices; evaluating and refining educational strategies to ensure alignment with policies, procedures, protocols, and long-term organizational goals; and driving a culture of collaboration, continuous learning, and innovation, leveraging several teaching modalities to shape the future of continuous learning and improvement. Drives regulatory compliance by: providing consultation using expert knowledge and strategic insight to ensure comprehensive compliance across the department; leading and/or advising on strategic initiatives and regulatory compliance efforts with a focus on ensuring sustainability and strategic alignment; developing, implementing, and revising policies, procedures, protocols, and educational programs to drive long-term regulatory excellence; and anticipating and mitigating future regulatory risks, shaping strategic compliance initiatives for organizational success.
Clinical Director ACESClinical DirectorPittsburg, CA$105,000–$110,000 / yearDeveloping and monitoring SV cases loads and capacity: Update SV Capacity sheet, assisting in monitoring credentialing, assigning distribution of caseload by time of day, region, qualifications, facilitating case transfers as needed, communicate SV needs to Recruiting. Working under the supervision of the Regional Director and in concert with department heads and the executive team, essential job responsibilities include, but are not limited to: Utilization Management: Conduct Daily and weekly reviews and problem solving with supervisors of client utilization for collective office and at individual client level.
NewAssistant Director for Clinical Research Programs UCSF Medical CenterAssistant Director for Clinical Research ProgramsSan Francisco, CAJob Summary: Under the supervision of the Associate Director for Clinical Research Programs, the Assistant Director, Clinical Research Operations, oversees the day-to-day staffing operations of their assigned research programs, including Clinical Research Managers, Clinical Research Supervisors and/or senior staff. The Assistant Director will manage 4 - 5 direct reports at the Clinical Research Manager (Clin Rsch Supv 2), and Clinical Research Supervisor (Clin Rsch Supv 1) levels, provide management oversight of approximately 20-25 FTE clinical research staff (Clinical Research Supervisors, Sr.
Clinical Research Manager UCSF Medical CenterClinical Research ManagerSan Francisco, CAThe Clinical Research Manager will work closely with senior management, including Principal Investigators, the Program Director, and Department leadership, to develop long and short term strategies to carryout the goal of developing effective treatments for Alzheimer's Disease, Progressive Supranuclear Palsy, Frontotemporal Dementia and other related disorders. To further engage in this work, the center collaborates with organizations such as the Alzheimer's Disease Research Center (ADRC), Bluefield Project to Cure Frontotemporal Dementia, California Alzheimer's Disease Center, Global Brain Health Institute, and the Tau Consortium.
Clinical Applications Supervisor, Clinical And Molecular Pathology Stanford Health CareClinical Applications Supervisor, Clinical And Molecular PathologyPalo Alto, CA$66.52–$88.14 / hourThe Supervisor- IT Applications provides day-to-day operational leadership for technical staff administering one or more information technology and systems functions supporting Stanford Healthcare/Medicine's business processes and technical platforms (including, Epic, Workday, Sectra, ServiceNow, Research, etc.). This role combines day-to-day people leadership with hands-on technical and operational expertise, serving as the first point of escalation for the team, while partnering with the Manager on staffing, scheduling, and broader service delivery outcomes, including supporting technical roadmap development.
Nurse Manager - Clinical Research Services UCSF Medical CenterNurse Manager - Clinical Research ServicesSan Francisco, CAThe clinical component of CTSI, Clinical Research Services (CRS) integrates the activities of multiple clinical research sites that provide adult and pediatric inpatient and outpatient clinical services to support the translation of promising clinical research ideas into successful protocols. UCSF's Clinical and Translational Science Institute's (CTSI) Clinical Research Services Unit (CRS) is recruiting for a Nurse Manager position to join their team whose mission is to provide high quality clinical research support to UCSF study teams.
Assistant Clinical Research Coordinator - Pediatric CHAMP Program UCSF Medical CenterAssistant Clinical Research Coordinator - Pediatric CHAMP ProgramSan Francisco, CADuties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The Assistant Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of two concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Clinical Research Coordinator Golden State DermatologyClinical Research CoordinatorContra Costa County, CAWe are a leading medical, surgical, and cosmetic dermatology group specializing in skin, hair, and nail conditions, Mohs micrographic surgery for the treatment of skin cancer, surgical and non-surgical cosmetic skincare, anti-aging, body contouring, and plastic surgery. Responsibilities include study start-up and regulatory activities, participant recruitment and study visits, source documentation and EDC entry, safety reporting, study supply management, monitoring visit preparation, and study close-out.
Clinical Research Coordinator - Division of HIV UCSF Medical CenterClinical Research Coordinator - Division of HIVSan Francisco, CAIncumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The CRC will conduct screening and enrolling study participants, scheduling study visits, and will conduct all participant facing procedures including gaining informed consent, training and supporting participants on the use of the technology associated with the study, conducting study surveys, performing finger-pricks for blood spot collection, and conducting non-invasive measurements of body composition such as height, weight, waist and hip measurements.
Senior Clinical Trial Manager - Job ID: 2020 Ascendis PharmaSenior Clinical Trial Manager - Job ID: 2020Palo Alto, CARemote$160,000–$170,000 / yearManages and/or supports vendor management for central laboratory, central IRB, central imaging, patient concierge services, and site payment systems including but not limited to: portal access management for sites and internal teams, report review, sample tracking, metrics review, document reviews and meeting participation. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Clinical Research Coordinator I - National Center for PTSD Palo Alto Veterans Institute for ResearchClinical Research Coordinator I - National Center for PTSDMenlo Park, CAKnowledge of VA and its health care system regarding clinical research trials and understanding of VA procedures and safety regulations; Experience with mobile and/or web analytics, dashboards, and/or processing of JSON data streams; Experience working with behavioral, mental health, and/or electronic health record data, especially using VA systems; Experience with additional data processing technologies including Python, SQL, Visual Studio, Azure, and/or AWS; Experience with AI and machine learning, particularly for behavioral data analysis; Data visualization skills. Knowledge and experience with web-based project management programs; Good interpersonal skills and strong collaborative attitude and capacity to interact with people; Strong organizational skills; Ability to work well both independently and in a collaborative team; Good writing skills and ability to develop periodic reports on program activities; Knowledge of research study protocols and IRB procedures; Knowledge and experience with manuscript development and literature review.
Clinical Research Coordinator I - The Nallamshetty Lab Palo Alto Veterans Institute for ResearchClinical Research Coordinator I - The Nallamshetty LabPalo Alto, CADegree in related field; Experience with grants and contracts function, clinical trial and research data management; Experience coordinating clinical research studies, recruiting research participants, collecting research data, and working with regulatory requirements; Knowledge of clinical research principles, Good Clinical Practice (GCP), human subjects protections, and research ethics gained through education or experience is desired. The position works closely with the Principal Investigator, study team, sponsors, regulatory bodies, and research participants to ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and federal regulations.