Clinical Research Assistant – Health Educator PAVIRClinical Research Assistant – Health EducatorMenlo Park, CATemporaryQUALIFICATIONS:Required: Bachelor's degree or equivalent experience;At least 1 year of relevant research experience (can be undergraduate experience);Preferred: Master's degree; Previous experience working in the VA system and/or experience with intervention trials in oncology, subject recruitment and screening;Understanding of statistics and familiarity with STATA or similar data analysis software;Strong interpersonal skills. With assistance from the PI, Dr. Manali Patel, the Health Educator will perform data collection, data entry, data management, simple data analysis, and creation of reports for funders as well as peer reviewed publications.
NewClinical Research Coordinator I – The Nallamshetty Lab PAVIRClinical Research Coordinator I – The Nallamshetty LabPalo Alto, CAFull timeQUALIFICATIONS Required: Bachelor's degree (or equivalent experience);Valid Driver License required;0-2 years of experience supporting clinical research, healthcare, laboratory, or related scientific environments;DesiredDegree 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.
Health Plan Enrollment Analyst Integrated Resources, IncHealth Plan Enrollment AnalystSan Francisco, CaliforniaContractorThis position is responsible for developing and overseeing the processes ensuring that all billing providers (approximately 2000) at Client and affiliates are appropriately and accurately credentialed and enrolled into all commercially contracted health plans, Medicare, Medi-Cal and Tricare which is required to appropriately generate revenue (approximately $500 million annually) in the course of patient care. Minimum of 8-10 years of work experience in healthcare environment with specific emphasis in provider enrollment, managed care, health plans affairs at an academic medical center and/or medical staff operations.
NewMechanical Engineer Stark Pharma Solutions IncMechanical EngineerFremont, CAWe provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. The role will focus on disposable medical devices, prototype development, design controls, testing, and cross-functional engineering support.
NewSFO- Airport Duty Manager AIRPORT MINORITY ADVISORY COUNCILSFO- Airport Duty ManagerSF, CA$149,656–$190,996 / yearFull timeCoordinate scheduling, scope of work and safety issues with stakeholders on all construction and maintenance projects to insure minimal operational disruption; monitor all construction activity occurring in "active" terminals to address safety and customer satisfaction concerns; conduct safety spot checks of all Airport facilities; respond, assess, and fix security issues to prevent violations and fines as related to Code of Federal Regulations (CFR) 1540-1542.Respond and manage the airport facility including the Emergency Operations Center during emergencies; coordinate support activities for routine and non-routine situations requiring the cooperation of federal, state, and local agencies; assist SFPD-AB with managing the transient program by actively monitoring facilities, admonishing individuals, signing citizen arrest forms, updating the Airport's data file, and appearing in Court. Manage tarmac delay program to ensure compliance with Federal guidelines by interacting with Federal Aviation Administration (FAA) and airlines to provide alternate gates and/or bus operations; monitor ground transportation traffic flow to ensure sufficient resources for customers and help enforce provider compliance; and monitor AirTrain and BART services to ensure service levels and resolution of outages; monitor the issuance of Notice to Airmen (NOTAMS) to reflect changing airfield conditions and/or hazards to air traffic.
Medical Publications Lead Cell Therapy | Scientific Communications Pyramid Consulting, IncMedical Publications Lead Cell Therapy | Scientific CommunicationsFoster City, CARemote$40–$45 / hourBy applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Immediate need for a talented Medical Publications Lead – Cell Therapy | Scientific Communications .
NewPrincipal Data Science/AI Product Manager Nesco Resource, LLCPrincipal Data Science/AI Product ManagerSouth San Francisco, CA$40.53–$92.63 / hourThis role partners with Data Science, Engineering, IT, and Product leadership teams to define AI product vision, develop roadmaps, and deliver intelligent solutions that enable proactive decision-making, automation, and personalized customer experiences. Client is seeking a Principal Data Science/AI Product Manager to lead the strategy, development, and delivery of AI/ML product capabilities that support customer engagement and business decision-making across Commercial, Medical, and Government Affairs functions.
Human Factors Engineer LancesoftHuman Factors EngineerMilpitas, CA$60Duties: Experienced R&D Engineer_Human Factors to apply human factors and ergonomics expertise to the definition, design, and evaluation of products within the R&D division of Diabetes Care;apply knowledge of human factors principles (human performance and limitations perceptual, cognitive, motor skills, anthropomorphic) and techniques (knowledge acquisition, user-interface design, usability evaluation) to diabetes care systems product development; Deliverables include, but are not limited to: Usability engineering files; Task analyses; Usability risk analyses; Usability testing throughout the product development process, from formative testing of early prototypes through usability validation of final designs. Proven ability to apply user-centered design and human factors/usability engineering principles to product research, development and design;experience in medical device development; Proven ability to quickly assimilate advanced domain knowledge and guide program teams on Human Factors strategy, HF deliverables for program scope, research strategy across the product development lifecycle and successful deliverable completion within project timelines.
NewClinical Trial Planning Specialist Planisware Pyramid Consulting, IncClinical Trial Planning Specialist PlaniswareFoster City, CARemote$50–$55 / hourBy applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Maintain accurate dependencies across Clinical Operations, Data Management, Regulatory, Biostatistics, Medical Affairs, CROs, and other functions.
Quality Engineer III LancesoftQuality Engineer IIISanta Clara, CA$45Managing strategic program for RA audit preparedness including anticipatory identification of risks, mitigation of risks identified during the audit process, and preventive actions for risks. This role will provide quality system and compliance support to the Regulatory Affairs (RA) organization by Driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metrics.
NewManufacturing Engineer Stark Pharma Solutions IncManufacturing EngineerFremont, CAWe provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. Ensure manufacturing processes, documentation, and training materials align with FDA and ISO 13485 requirements.
AD, Medical Communication & Publications Rigel Pharmaceuticals, Inc.AD, Medical Communication & PublicationsSouth San Francisco, CA$160,000–$195,000 / yearEnsure all assigned Rigel-sponsored publications are developed according to Rigel publication policy and good publication practice, including published guidelines (e.g., GPP2022, ICMJE, CONSORT) and ensure all required documentation has been recorded in publication tracking system (eg, PubsHub). This person is responsible for supporting development of a comprehensive, cross functionally aligned strategic publication plan and leading the planning, development, and publication of manuscripts, abstracts, posters, and other scientific materials to ensure that all timelines are met.
Director, Distribution & Trade Rigel Pharmaceuticals, Inc.Director, Distribution & TradeSouth San Francisco, CA$195,000–$235,000 / yearThe Director of Distribution & Trade is responsible for providing strategic leadership and operational oversight for the company's distribution network, including third-party logistics (3PL) providers, specialty distributors, and specialty pharmacies. Collaborate closely with Patient Services, Supply Chain, Finance, Legal, Regulatory Affairs, Quality, and Commercial Operations to ensure efficient distribution processes.
Principal Experience Designer Tranzeal Inc.Principal Experience DesignerSouth San Francisco, CAThis combined team, in collaboration with key partners, builds solutions to serve Marketing, Customer Engagement, Medical Affairs, Public Affairs & Access ( "CMG ), and other patient- and customer-facing teams across CMG to shape and drive a seamless, consistent, meaningful, and compliant experience for patients and customers across our interactions. As healthcare evolves, we are bold in our approach leveraging cutting edge AI, advanced digital engagement, end-to-end content management, and omnichannel technologies and operations to create seamless, personalized, and meaningful experiences for our patients and customers.
Supply Chain Director Russell Solutions GroupSupply Chain DirectorMenlo Park, CAThe Supply Chain Director or Manager is responsible for developing, implementing, and optimizing Inquis Medical's end-to-end supply chain strategy to ensure the timely, cost-effective, and compliant delivery of materials, components, and finished medical devices. This is a hands-on position that will partner closely with Engineering, Quality, Regulatory Affairs, Operations, Clinical Affairs, Finance, and external suppliers to support product development, commercialization, and ongoing manufacturing operations.
NewVice President, Translational Medicine & Clinical Pharmacology Rigel Pharmaceuticals, Inc.Vice President, Translational Medicine & Clinical PharmacologySouth San Francisco, CA$306,000–$365,000 / yearLead clinical pharmacology strategy and development plans for Rigel assets, including ADME, drug-drug interactions (DDIs), pharmacokinetics/pharmacodynamics (PK/PD), exposure-response, bioavailability/bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. Advanced scientific degree (PhD, PharmD, MD, or equivalent) in pharmacology, pharmaceutical sciences, drug metabolism, toxicology, translational medicine, or a related discipline; PhD or PharmD strongly preferred for a clinical pharmacology-focused role.
QA Documentation Specialist-I Integrated Resources, IncQA Documentation Specialist-IFoster City, CaliforniaFull timeCarefully document testing and audit results in Quality Assurance Logs and process records, and shared test results with production workers, supervisors and managers to identify and implement solutions. Adept at managing and mitigating risk, using a proactive approach to identify issues and collaborate with leaders to create and implement corrective action.
Materials Science Specialist Tucker Parker Smith Group (TPS Group)Materials Science SpecialistSan Rafael, CAThis position will support regulatory commitments and CAPA activities by reviewing, updating, and implementing raw material specifications in accordance with current compendial, quality, and internal requirements. Required Qualifications Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline.
Director, RA Gateway RecruitingDirector, RASan Francisco, CAManage and prepare post-market filings and product safety reports (e.g., Annual Reports, DSUR, PSUR, REMS Annual Report, Supplements, Technical Documentation File lifecycle maintenance, responses to regulatory information requests). Experience with commercial products, Drug Safety/ Pharmacovigilance (adverse event reporting, DSUR, PSUR, REMS Annual Reports and audits), product approval process, and post-market surveillance.
GxP Project Manager Katalyst Healthcares & Life SciencesGxP Project ManagerSan Francisco, CAThe Project Manager will collaborate with Quality, Manufacturing, Validation, IT, Regulatory Affairs, Engineering, and external vendors to successfully deliver projects on schedule, within budget, and in compliance with regulatory requirements. We are seeking an experienced GxP Project Manager to lead and manage cross-functional GxP initiatives supporting pharmaceutical manufacturing, quality, laboratory, validation, and IT systems.