Manager of Research Clinic Kaiser PermanenteManager of Research ClinicOakland, CACoordinates and manages clinical research by: guiding and coordinating team in the preparation and submission of a portfolio of research proposals as applicable; guiding and coordinating team in the collection, management, analyses, and interpretation of clinical trials data; orchestrating internal resources needed to provide consultation on implementing clinical trials for staff; influencing the development and implementation of policies and procedures for developing research protocols and other processes of clinical trials; overseeing the preparation, submission, and/or compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for training others to execute 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 training others to support 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 planning the effective, long-term design of clinical trial applications to ensure compliance with all applicable federal, state, and local regulations and KP policies and procedures within unit or team; developing guidance for identifying and resolving compliance and/or quality issues and developing corrective action plans; developing and socializing updates for compliance-monitoring/audit systems and documentation; leading the implementation of new or updated research protocols, procedures, and guidance to ensure confidentiality, privacy, and security of clinical research data; driving the implementation of research protocols, procedures and guidance to ensure confidentiality, privacy, and security of clinical research data within unit; and overseeing and advising team members who are providing guidance and partnering with investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines.
Clinical Rehabilitation Operations & Patient Experience Director HireNow StaffingClinical Rehabilitation Operations & Patient Experience DirectorLos Gatos, California$100,000–$120,000 / yearHireNow Staffing is recruiting a Clinical Rehabilitation Operations & Patient Experience Director who demonstrates the following: Possesses at least five years of progressive healthcare leadership or rehabilitation operations management experience. This full-time leadership opportunity is ideal for an experienced healthcare operations professional who excels at building high-performing clinical teams, optimizing operational performance, and delivering exceptional patient outcomes.
Medical Director, Clinical Informatics, Anesthesia Sutter HealthMedical Director, Clinical Informatics, AnesthesiaSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Working knowledge of the clinical care information systems implementation process, integration of workflows, use and support methodologies, regulatory requirements, strategic and tactical planning, project leadership/management and group dynamics.
Medical Director, Clinical Informatics, Medical Specialties Sutter HealthMedical Director, Clinical Informatics, Medical SpecialtiesSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Working knowledge of the clinical care information systems implementation process, integration of workflows, use and support methodologies, regulatory requirements, strategic and tactical planning, project leadership/management and group dynamics.
Medical Director, Clinical Informatics, Surgical Specialties Sutter HealthMedical Director, Clinical Informatics, Surgical SpecialtiesSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Working knowledge of the clinical care information systems implementation process, integration of workflows, use and support methodologies, regulatory requirements, strategic and tactical planning, project leadership/management and group dynamics.
Medical Director, Clinical Informatics, Behavioral Health Sutter HealthMedical Director, Clinical Informatics, Behavioral HealthSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Working knowledge of the clinical care information systems implementation process, integration of workflows, use and support methodologies, regulatory requirements, strategic and tactical planning, project leadership/management and group dynamics.
Medical Director, Clinical Informatics, Emergency Medicine Sutter HealthMedical Director, Clinical Informatics, Emergency MedicineSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Total compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs.
NewAdolescent Mental Health Clinical Expert (Contract) Vals AIAdolescent Mental Health Clinical Expert (Contract)San Francisco, CaliforniaClinical training and professional credentials are required , such as LCSW/LICSW, LMFT, LPC/LPCC/LCPC, clinical psychologist, psychiatrist, MD/DO, or comparable clinical mental health credentials. You’ll bring clinical judgment to reviewing AI conversations, identifying safety risks, and helping define what appropriate model behavior looks like.
Head Of Clinical Pharmacology Structure Therapeutics IncHead Of Clinical PharmacologySouth San Francisco, CA$275,000–$360,000 / yearThe company's 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. Proven ability to manage vendor performance and stakeholder relationships while making evidence-based decisions in fast-paced, global clinical development environments, supported by strong analytical, regulatory, negotiation, and communication skills.
Head of Clinical Pharmacology Structure Therapeutics IncHead of Clinical PharmacologySouth San Francisco, CA$275,000–$360,000 / yearClinical Pharmacology leadership experience representing the function in both strategic and scientific team settings Cross-functional leadership experience and supervisory experience Clinical Pharmacology experience with small molecules and metabolism In-depth knowledge of relevant global regulatory requirements and guidelines related to clinical pharmacology studies, including FDA, EMA, and ICH guidelines. The company's 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.
Systems Administrator III, Inpatient Clinical Documentation, Inpatient Procedure Orders, OPA Kaiser PermanenteSystems Administrator III, Inpatient Clinical Documentation, Inpatient Procedure Orders, OPAPleasanton, CAEssential Responsibilities: Completes work assignments by applying up-to-date knowledge in subject area to meet deadlines; following procedures and policies, and applying data and resources to support projects or initiatives; collaborating with others, often cross-functionally, to solve business problems; supporting the completion of priorities, deadlines, and expectations; communicating progress and information; identifying and recommending ways to address improvement opportunities when possible; and escalating issues or risks as appropriate. The System Administrator III, Health Systems (Inpatient Clinical Documentation, Inpatient Procedure Orders, OPA) supports the Clinical Care and Patient Engagement Technologies organization by serving as a senior-level subject matter expert responsible for the analysis, design, build configuration, implementation, optimization, and ongoing support of Epic applications with a minimum of 4-5 years of build experience.
Global Clinical Trial Leader Compass ConsultingGlobal Clinical Trial LeaderSouth San Francisco, CARole & Key Responsibilities: Study Execution & Team Collaboration: Operational Expertise: Provide operational guidance to one or more global cross-functional Protocol Execution Teams (PETs) across all study stages (start-up, conduct, and close-out). Trial Documentation: Drive and finalize cross-functional activities ensuring the quality delivery of vendor specifications, drug supply forecasting, monitoring/communication plans, Trial Master Files (TMF), and CTMS data.
Global Clinical Trial Leader LancesoftGlobal Clinical Trial LeaderSouth San Francisco, CA$92Trial Documentation: Drive and finalize cross-functional activities ensuring the quality delivery of vendor specifications, drug supply forecasting, monitoring/communication plans, Trial Master Files (TMF), and CTMS data. The CTL actively contributes to the Protocol Execution Team (PET), manages vendors, develops risk mitigation strategies, and champions change related to study assignments and department goals.
Clinical Lab Supervisor - San Rafael, CA Planned Parenthood Northern CaliforniaClinical Lab Supervisor - San Rafael, CASan Rafael, CA$133,200–$165,200 / yearWe provide a full range of services, including birth control, breast exams, cancer screenings, medication and in-clinic abortion, pregnancy testing and counseling, prenatal care, PrEP, and nPEP to prevent HIV infection, STI screening and treatment, vasectomy and infertility services, gender-affirming hormone therapy, and more. The Technical Supervisor of the High Reference Laboratory will report to the Chief Medical Officer/Chief Operating Officer with a dotted line to the Senior Director of Clinical Quality Assurance and will manage a team of CLS and CLA individuals.
NewRegional Clinical Director Titan Placement GroupRegional Clinical DirectorSan Francisco, CAWe’re hiring a Regional Clinical Director in Northern California (Bay Area) or Southern California who wants to shape the future of behavioral healthcare while leading high-performing clinical teams serving adults with severe mental illness. You’ll partner with operational and medical leadership to drive clinical excellence, improve patient outcomes, supervise multidisciplinary teams, and support the continued growth of innovative behavioral health programs.
Documentation Systems Manager Integrated Resources, IncDocumentation Systems ManagerFoster City, CaliforniaFull timeJob DescriptionTitle: Documentation Systems Manager Duration: 6 Months Location: Foster City, CA The Documentation Systems Manager, Corporate Engineering provides technical leadership and accountability for all documentation systems maintenance for the engineering and research and development (R&D) laboratories, clinical manufacturing related facilities, warehouses, and office buildings at Client's Corporate Headquarters in Foster City, CA. Develops, implements, and maintains documentation programs and processes to ensure high quality of operations, and compliance with UBC, UFC, NEC codes, current Good Manufacturing Practices (GMPs), Good Engineering Practices (GEPs) and Good Laboratory Practices (GLPs).
Operations Manager, CRS UCSF Medical CenterOperations Manager, CRSSan Francisco, CAOther responsibilities for the Operations Manager include but are not limited to: Organizing multi-layered interviews for faculty recruitments; Facilitating logistics for Center meetings, retreats, and/or events; Drafting and editing high-level correspondences as directed by leadership; Acts as a central liaison for information related to the department for both ancillary departments and external organizations, as needed; Manage on-boarding logistics and coordination for both faculty and staff hires, as well as serving as the main point of contact for operational activities in CRS. Department Summary: The Department of Obstetrics, Gynecology and Reproductive Sciences (Ob, Gyn & RS) is a major academic Department in the School of Medicine, engaged in clinical, research and training activities at the Parnassus, Mount Zion, and Zuckerberg San Francisco General Hospital campuses, the new Betty Irene Moore Women's Hospital at Mission Bay, as well as satellite locations throughout the Bay Area, with an annual operating budget of $149 million.
Clinical Laboratory Scientist Generalist Sutter HealthClinical Laboratory Scientist GeneralistOakland, CA$66.36–$82.88 / hourKnowledge of laboratory test methods, specimen requirements, test limitations, test interpretations sufficient to perform tests accurately and to recognize and analyze problems effectively. Position Overview: This position may be required to perform tests in all areas of the Clinical Laboratory including, but not limited to: Blood Bank, Hematology, Chemistry, Coagulation, Urinalysis and limited Microbiology.
Clinical Trials Management Associate – II Integrated Resources, IncClinical Trials Management Associate – IIFoster City, CaliforniaContractorInterfaces with individuals in other functional areas to address routine study issuesAbility to develop tools and processes that increase measured efficiencies of the projectMay be asked to assist in the training of CTMAs and CPAsAssists in CRO or vendor selectionCoordinates CROs or vendorsAssists in the setting and updating of study timelinesMust be able to participate in departmental or interdepartmental strategic initiatives under general supervisionAssists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepanciesMay conduct site evaluation, initiation, co-monitoring, and closeout visits in addition to routine monitoring visits, as requiredAssures site compliance with the protocol and regulatory requirementsDrafts and coordinates review of protocols, informed consents, case report forms and monitoring plansExcellent verbal, written, interpersonal and presentation skills are requiredKnowledge of FDA and or EMA Regulations, ICH Guidelines, and GCP governing the conduct of clinical studiesWorking knowledge and experience with Word, PowerPoint and ExcelQualificationsAt least 3+ years of experience and a BS or BA in a relevant scientific disciplineFeel free to forward my email to your friends/colleagues who might be available. Job DescriptionMust meet all requirements for CTMA position and have demonstrated proficiency in all relevant areasMust be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and proceduresParticipates or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teamsMust be able to anticipate obstacles and proactively develop solutions to achieve project goalsMust have a general understanding of functional issues and routine project goals from an organizational perspectiveMay participate in abstract presentations, oral presentations and manuscript development.
Lead Account Manager - San Francisco, Bay Area CA Thermo Fisher Scientific IncLead Account Manager - San Francisco, Bay Area CASouth San Francisco, CA$129,600–$194,000 / yearWe provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.