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ProKatchers is seeking a travel nurse RN Quality Assurance for a travel nursing job in Novato, California.. Posted job title: (RN) - Quality assurance. Founded in 2016, ProKatchers Inc. is a JCC-certified organization and a recognized leader in healthcare staffing.. Named one of the Fastest Growing Healthcare Staffing Firms by Staffing Industry Analysts (SIA) for 2023–2024, we are proud to be among the top-rated companies in our industry.. We specialize in placing clinical and allied health professionals in a wide range of healthcare settings, including acute care hospitals, skilled nursing facilities, long-term care centres, rehabilitation facilities, behavioural health canters, home and community health programs, urgent care clinics, and more.
LanceSoft is seeking a travel nurse RN Quality Assurance for a travel nursing job in Novato, California.. Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization.. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022.. We understand the importance of partnering with an expert who values your needs, which is why we’re 100% committed to finding you an assignment that best matches your career and lifestyle goals.. LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.
Job Posting: Pharmacy Operations Manager Location: San Francisco, CA Job Type: Full-Time Overview: We are seeking a Pharmacy Operations Manager to lead the daily operations of our fast-paced pharmacy department in San Francisco, CA. This role is ideal for an experienced pharmacy professional with strong leadership skills, a deep understanding of regulatory compliance, and a passion for delivering high-quality patient care.. Responsibilities: Oversee daily pharmacy operations to ensure efficient workflows and exceptional patient care.. - Foster a culture of patient safety, collaboration, and high service standards.. If youre ready to make a meaningful impact in pharmacy management, we want to hear from you!. Contact: Thomas Tatham thomas.tatham@soliant.com
Case Management/Utilization Review Admission Criteria Benefits Eligibility Care coordination Data Abstraction. Needs Assessment/ Order DME Plan of Care Prior Authorizations Utilize InterQual Criteria. Regulatory CMS: Centers for Medicare and Medicaid Services CPT (Current Procedural Terminology) coding and billing. NCQA (National Committee for Quality Assurance). OSHA: Occupational Safety and Health Administration The Joint Commission/ Core Measure/National Safety Goals Worker’s Compensation *
We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.. The S&E team interacts with biotech and biopharma companies, academic institutions, venture firms, and other stakeholders from the life sciences industry ecosystem, for exploration of potential opportunities to collaborate, in-license, out-license, invest into- or acquire assets.. Proactively search for, identify, and evaluate potential opportunities (research collaboration, in-licensing preclinical and clinical assets, platform technologies and research tools) that are consistent with external BD strategies for the advancement of AbbVie’s Specialty TA pipeline and Discovery Platforms strategy, and driving sustainable growth for the Company.. Doctorate degree in a related scientific field required (e.g. PhD, PharmD, MD).. Must possess a solid foundation in drug discovery processes, with in depth knowledge of at least one aspect of Drug Development (e.g., pre-clinical research, clinical development, Regulatory Affairs, Chemistry Manufacturing and Controls (CMC
The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer.. The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.. Knowledge of medical/oncology process and terminology; experience and knowledge of IRB policy and procedure; background in science/medicine, preferably in hematology/oncology.. Prior experience with UCSF, particularly with research in the oncology setting, clinical trial billing, and institutional policies for study compliance and regulation.. The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
Drive the overall planning, execution, and delivery of assigned drug development programs from candidate nomination through early clinical trials.. Support the Project Team Leader (PTL) on cross-functional Project Development Teams (PDTs), including Clinical, Regulatory, Toxicology, Pharmacology, Assay Development, CMC, Research and Strategy, ensuring clear roles, responsibilities, and accountability.. Expertise in the use of modern project management tools (Gantt charts, risk logs) and technologies (Smartsheet’s, Excel, PowerPoint, ThinkCell).. TCG Labs-Soleil, established in partnership with The Column Group , a science-focused venture capital firm, is pioneering a novel ‘venture capital-biotech’ model.. This model supports scientific entrepreneurs from the initial idea to clinical proof of concept (PoC) by combining a dedicated fund (TCG Labs) with our independent, evergreen R&D center led by a top-tier scientific team (Soleil).
Our mission is to make it radically easier, faster, and more affordable to generate high-quality real-world evidence.. Founded in 2014, we’ve raised $100M+ from top investors like Amplify Partners, Felicis Ventures, B Capital Group, and Y Combinator.. You will blend deep knowledge of the clinical research space with operational excellence and a bias towards innovation, helping shape and scale our tech-forward, AI-powered approach to real world evidence generation.. Bachelor's degree, preferably in life science area or public health, along with 5 years working in the clinical trials/research industry, with at least 2 years leading and managing full-service research studies;. Trials are a major bottleneck in drug development, and the promising advancements in biotech cannot achieve their full potential unless clinical research becomes more effective.
We are a global management consulting firm that specializes in strategy, marketing, pricing, and sales. Our Healthcare & Life Science Division works across the highly innovative, complex healthcare sector, including pharmaceuticals & biotech, medical technology, diagnostics, digital health & healthcare IT, healthcare B2B, providers, consumer health, and animal health. Entrepreneurship is a powerful force that drives the growth not only of our firm but our clients and people. Project Support: Collaborate with project teams to support various client engagements, including developing presentations, creating financial models, and contributing to client workshops. Has obtained or is currently enrolled in an undergraduate or graduate degree program at an accredited university/college pursuing a degree in biology, chemistry, biochemistry, or pharmacology, or a related sciences or business field
Our program seeks to build cohorts of academic investigators with ongoing projects that are at any stage in drug development between having a validated target and ready to enter clinical trials.. We are seeking a highly motivated and innovative individual to join our team as a Learning Experience Designer.. The ideal candidate will have a background in biomedical research, learning experience design, or instructional design, and a passion for designing content that fosters a dynamic and inclusive learning environment.. Masters degree or higher in a scientific field (e.g., Pharmacology, Biotechnology, Molecular Biology, Chemistry, or related discipline) and 2+ years of experience in science education.. OR bachelors degree in Instructional Design, Learning Experience Design, with demonstrated knowledge of scientific research and drug development (certificates, courses, or experience)
Under direction of the Chief Information Officer (CIO), the Associate Chief Information Officer (ACIO) will provide the technological, informational vision and leadership for the organization.. Electronic Health Records (EHR) Management: Oversee the implementation, optimization, and maintenance of EHR systems to ensure they meet the needs of NEMS mission, providers, and patients.. Leads the development and implementation of clinical informatics programs including Computerized Physician Order Entry (CPOE), Knowledge Based Charting (KBC), Clinical Decision Support (CDS), and Electronic Health Record (EHR).. Regulatory Compliance: Ensure that the FQHC’s IT systems and practices comply with federal, state, and local regulations, including HIPAA, HITECH (Health Information Technology for Economic and Clinical Health Act), and other relevant standards.. Working knowledge of Center for Medicare and Medicaid Services (CMS), Health Resources and Services Administration (HRSA), and other State and local programs, as appropriate, or needed.
Perform data review supported by Clinical Research Scientist(s) (CRS), participate in protocol deviation meeting that will occur monthly or as needed.. Create or support the creation of relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents, and scientific publications.. Successful completion of MD training mandatory; 3 years of clinical experience in treating oncology patients or a completed fellowship in a Hematology-Oncology program.. 8 years of combined experience in oncology clinical research and drug development in academic and/or industry, including experience as a medical monitor and (sub)investigator in oncology clinical trials.. 3 years in industry leadership as medical lead for an oncology development program(s) with direct or indirect management of cross-functional areas (e.g., clinical operations, biostatistics, data management, biomarker, pharmacovigilance, quality, etc.)
The IT Senior Manager, R&D and Quality Systems is responsible for implementing and supporting R&D and quality business systems required for drug development in the cGMP environment. This position is responsible for the business analysis, planning, project management, implementation, computer systems validation and ongoing support of business applications in the areas of Research & Development Analytical, Regulatory Affairs, Clinical, Quality Affairs and Quality Control. Manages the application support of R&D and Quality systems to ensure they meet business needs and user requirements, remains in compliance per cGMP requirements and GAMP5 guidelines. Experience with R&D, Brand, Quality Assurance / Quality Control, Regulatory Affairs, Clinical, Manufacturing environments regulated by the FDA. Experience with Waters CDS, Trackwise, LIMS, Electronic Regulatory Filing System, Document Management, Quality Systems, Laboratory Operations.
Director/Senior Director, Scientific Affairs.. Reporting to the Executive Director of Scientific Affairs, this individual will be responsible for internal and external scientific and clinical research initiatives under the Medical Affairs umbrella. Collaborates across all appropriate functional groups to support ongoing clinical trials, medical and scientific affairs research initiatives, and other scientific affairs activities for the adult hepatology program. Experience with scientific and medical writing for regulatory documents, scientific publications, congresses, research forums and other core scientific communications deliverables. Rare disease, liver or gastroenterology disease experience is a plus.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need.. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.. Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes.. CONTACTS : Clinical Medical Writing, Biostatistics, Clinical Data Management, Statistical Programming, Clinical Operations, Medical Affairs, Medical Directors, Regulatory Affairs, Legal, Commercial, Pharmacology/Toxicology, Corporate Compliance, Project management, Pharmacovigilance.. Basic understanding of the concepts of coding dictionaries (MedDRA, WHO Drug).
The Senior CSL works closely with key stakeholders and collaborates with colleagues across Roche/Genentech to streamline processes, identify synergies, and maximize efficiency. Your primary responsibility as a Senior CSL will be to provide strategic, technical, and operational leadership for the design, implementation, and lifecycle management of clinical systems, including but not limited to Interactive Response Technologies (IRT/IxRS) and electronic Clinical Outcome Assessments (eCOA) across the ECD portfolio at both study and program levels. Collaborate with a cross-functional team of internal stakeholders—including but not limited to Clinical Operations, Biostatistics, Clinical Supply Chain, Data Management, and Procurement—and clinical systems vendors to ensure successful implementation and maintenance of technology solutions supporting clinical trials. Lead Clinical Scientist, Hematology/Oncology Consultant – Healthcare Performance Improvement (Clinical Documentation Integrity) Clinical Content Lead – Oncology, Informatics & Data Tools - Manta Cares Senior Director, Clinical Research - Oncology Medical Director, Clinical Platform & Innovation Sr. Director, Clinical Research - Oncology (Sr. Medical Director) San Mateo County, CA $275,000.00-$325,000.00 2 weeks ago.. Associate Director, Clinical Operations - Oncology (Compound Lead) Director, Clinical Biomarker, Late Stage Neurology (Translational Medicine) Executive Director, Head of Clinical Quality Assurance Millbrae, CA $252,000.00-$275,500.00 1 week ago
Employee Assistance Program (EAP) including free counseling and health coaching.. We offer ongoing training and development opportunities for licensed and unlicensed healthcare team members, and have best in class clinical resources for training, education, and point of care support. The Assistant Director of Nursing (ADON) is responsible for managing and supervising the nursing staff and operations of the facility to ensure that patients receive appropriate healthcare services. The ADON also ensures compliance with regulatory guidelines and maintains a safe and healthy environment for patients and staff. Regulatory agency knowledge including The Joint Commission, DHSS, Centers for Medicaid/Medicare Services is preferred.
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. Contacts: Clinical Medical Writing, Biostatistics, Clinical Data Management, Statistical Programming, Clinical Operations, Medical Affairs, Medical Directors, Regulatory Affairs, Legal, Commercial, Pharmacology/Toxicology, Corporate Compliance, Project management, Pharmacovigilance. Basic understanding of the concepts of coding dictionaries (MedDRA, WHO Drug). BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options. Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes. CONTACTS Clinical Medical Writing, Biostatistics, Clinical Data Management, Statistical Programming, Clinical Operations, Medical Affairs, Medical Directors, Regulatory Affairs, Legal, Commercial, Pharmacology/Toxicology, Corporate Compliance, Project management, Pharmacovigilance. Basic understanding of the concepts of coding dictionaries (MedDRA, WHO Drug).
Evidence of medical writing career development is desirable, e.g., American or European Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through the Drug Information Association.. Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.. Job function Job function Writing/Editing, Science, and Research. Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing. Technical Writer Veterinary Medical Devices Technical Writer Veterinary Medical Devices Associate Director, Clinical Medical Writing Associate Clinical Trials Management (Contract) Alameda, CA $158,000.00-$224,500.00 1 week ago