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The Nursing Supervisor RN oversees hospital nursing staff to ensure quality patient care and compliance with healthcare regulations.. Responsibilities include staff management, training, administrative reporting, budgeting, and coordinating nursing services across departments.. The Nursing Supervisor will also participate in program development and training for nurse-recruitment activities and assist with continuing education programs.. ScionHealth has a comprehensive benefits package for benefit-eligible employees that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.. nursing supervision, registered nurse, patient care management, hospital administration, staff training, healthcare compliance, budget management, nursing protocols, continuing education, hospital nursing services
This unique opportunity is at a prestigious facility looking to hire a traveling therapist. This exciting area offers many recreational activities. As a premier travel therapy company, Host Healthcare offers top pay, excellent benefits, and personalized service. The ideal candidate for this position will be dedicated to providing patients with the highest level of service. The ideal candidate will also be knowledgeable in Medicare, Medicaid, and private insurance, as well as the ability to complete relevant insurance documentations.
We are one of the largest private duty nursing companies in the nation and growing!. Pediatric Patient -G,T,V both AM shift and NOC Available!. Weekly and/or Daily Pay. Our homecare is always delivered from a place of heartfelt compassion and empathy, and every one of our Registered Nurses (RN)s works together to make sure we achieve outstanding clinical outcomes. As an employer accepting Medicare and Medicaid funds, employees must comply with all health-related requirements in all relevant jurisdictions, including required vaccinations and testing, subject to exemptions for medical or religious reasons as appropriate.
Our client is a major PBM (Pharmacy Benefit Services) entity owned by 20 non-profit health plans serving >33 million members and benefits manager of government programs including Medicare and Medicaid.. Performs prospective and/or retrospective drug utilization review and appeals per State and Federal regulations.. Provides prior authorization services for formulary drugs, develops programs to provide optimal pharmacy care to patients, participates in drug utilization review programs, reviews assessment and documentation of patient care, and retrospective reviews of provider reimbursement.. Maintains clinical skills and knowledge of pharmacotherapy by reviewing the literature, continuing education, and any company-provided in-services.. Education/Certifications: Rph or PharmD, Doctor Of Pharmacy, CA State Licensure – Pharmacy
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.. As a Scientist you will provide hands-on laboratory assistance to support pre-formulation, materials science, and compounding activities for small molecule, peptide, and antibody drug development projects.. Assist in studies such as solubility, characterization, and preclinical formulation development to support selection and optimization of developable candidates along with other pre-formulation/characterization studies.. Familiarity with the development and execution of chemical and instrumental methods (e.g. HPLC, Solubility Analysis, DSC, TGA, PXRD, Particle-Size Analysis, GVS, PLM, T3, and SEM) of analyses for development compounds, drug substances, raw materials, intermediates, drug products, and packaging materials.. The hourly pay range estimated for this position Specialist II, Clinical Lab Scientist based inCalifornia is –.
Join to apply for the Associate Director - Hematology, Oncology Data Sciences & Digital Health role at Johnson & Johnson Innovative Medicine. You will report to the Head of Hematology & Oncology Data Science.. Serve as primary business leader for Data Science & Digital Health programs for robust Hematology Oncology portfolio.. Work closely with individual clinical teams as well as functional area partners (e.g., Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making.. Advance degree in Health Science (Ph. D or MD) or Masters Degree, Pharm D with equivalent work experience in pharmaco-epidemiology, statistics, computational science, outcomes research or related field in health care area.
BioPhase is partnering with a cutting-edge biotech company to hire a Chief Medical Officer (CMO).. The CMO will drive clinical trial execution, collaborate with investigators and partners, and ensure alignment with business objectives.. Oversee clinical operations, medical monitoring, and regulatory affairs.. MD, MD / PhD with strong drug development experience.. 10+ years in biotech / pharma, with oncology experience preferred.
Join to apply for the Johnson & Johnson, Associate Director - Hematology, Oncology Data Sciences & Digital Health - Application via WayUp role at WayUp. Serve as primary business leader for Data Science & Digital Health programs for robust Hematology Oncology portfolio.. Work closely with individual clinical teams as well as functional area partners (e.g., Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making.. Advance degree in Health Science (Ph. D or MD) or Masters Degree, Pharm D with equivalent work experience in pharmaco-epidemiology, statistics, computational science, outcomes research or related field in health care area.. Associate Director, R&D Data Science and Digital Health - Immunology
The Chief Medical Officer, CMO will work as a strategic partner with other members of the senior executive team to develop and advance their clinical development strategy and drive the clinical research vision and regulatory roadmap for the company.. The CMO will have over-arching responsibility for the successful clinical development of the Companys pipeline programs and will be the external face of the company for clinical research and development opportunities, interacting with principal investigators, key opinion leaders, and potential pharmaceutical partners.. Actively assist in seeking product and/or technology alliances with appropriate pharmaceutical company partners to enhance/expedite the development of the companys assets.. Board Certified MD/PhD, or MD with medical research and drug development experience.. Prior experience in leading interactions with the FDA and knowledge of FDA/EMA GCP clinical requirements.
Join Bristol Myers Squibb as a Clinical Development Program Lead, Neuropsychiatry (Executive Director).. Position Summary : The Clinical Development Program Leader oversees the design and execution of clinical trials, manages teams of clinical professionals, and contributes to strategic planning and regulatory submissions.. Qualifications & Experience : MD or equivalent, with over 10 years of clinical trial and drug development experience, including management and regulatory expertise.. Additional Details : The role requires domestic and international travel, offers competitive compensation, and benefits aligned with industry standards.. The work environment emphasizes diversity, inclusion, and work-life balance.
We are a dynamic and innovative Cardiac Cath Lab Ambulatory Surgery Center, proudly accredited by AAAASF and committed to delivering the highest quality patient care.. Assistant Director of Nursing (ADON) Kearny Mesa. Assistant Director of Nursing (ADON) Arbor Hills. LVN Resident Services Director/ Assisted Living DON. Clinical Nursing Supervisor (RN) - Behavioral Health
The Regulatory Affairs Manager (RA Manager) will manage, evaluate, and complete regulatory projects consistent with company goals.. Represents Regulatory in cross-functional teams and provide guidance to teams on the regulatory requirements and risk(s) to support clinical development programs including preparation and maintenance of e.g., IND, CTA, and IMPD filings.. Collaboratively develop global regulatory strategies to support CMC, nonclinical, and clinical activities across various development programs.. Bachelor's degree in scientific discipline with 2-5 years pharmaceutical industry experience, including 2+ years in Regulatory Affairs.. Working knowledge of GMP, GLP, and GCP regulations as well as an understanding of the pharmaceutical product life cycle.
A global leader in medical technology is seeking an experienced and driven Regulatory Affairs Specialist / Manager to join their team in California.. Proven track record with successful 510(k), EU MDR, and PMA submissions. Ensure compliance with evolving regulations, including FDA Medical Device Regulations and EU-MDR, by supporting regulatory initiatives. Support business export control (BEC) listings, facilitating global product releases while maintaining compliance. Create a job alert for this search Regulatory Specialist
Quality Assurance Associate I, Analytical page is loaded Quality Assurance Associate I, Analytical Apply locations San Diego, CA time type Full time posted on Posted 2 Days Ago time left to apply End Date: August 8, 2025 (27 days left to apply) job requisition id 0089295 Quality Assurance (QA) Associate I, Analytical. We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, Good Manufacturing Practices (GMP) manufacturing and stability storage and testing as well as Clinical Supply Services.. A QA Associate I must be familiar with applicable GMP for quality standards.. Highly preferred to have experience with HPLC, HPLC data review and quality systems such as Trackwise and Empower. Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, on-site yoga and HIIT classes, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment.
RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein.. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.. In addition, the Associate Director of Clinical Standards & Processes will be tasked with tracking and ongoing Standard Operating Procedure/ Work Instruction (SOP/WI) review and updates as well as aligning with Quality Assurance (QA) to ensure Good Clinical Practice (GCP).. Fundamental knowledge of US, EU and international regulatory standards and guidelines for the conduct of clinical trials (ICH GCP, FDA; EMA; ANZ regulations). Strong knowledge/experience in vendor management, clinical operations and management of electronic Trial Master Files (Veeva eTMF).
With a focus on culturally sensitive, affordable services, TrueCare aims to improve the health of diverse communities.. Our vision is to be the premier healthcare provider in the region, delivering exceptional patient experiences through innovative, integrated care.. The Clinical In-Basket Nurse engages in managing the electronic health records (EHR) system, particularly focusing on the "In-basket.. Clinical Decision Support : Applying clinical knowledge to help resolve issues within the In- basket.. Data Entry and documentation : Ensuring that communications and care notes within the in basket are documented accurately using smart phrases in EPIC. Also, flagging important tasks to providers.
Ensures that all clinical research projects comply with Institutional Review Board (IRB) requirements, Good Clinical Practice (GCP) guidelines, and relevant federal regulations.. Ensure compliance with IRB requirements, DoD/NIH/FDA policies, and institutional procedures.. Strong working knowledge of project management software (e.g., MS Project, Smartsheet). · Experience with Department of Defense (DoD), NIH, CDC, or other federal research sponsors required.. · Clinical research certification (e.g., CCRC, CCRP) strongly preferred.
all related health care services activities, including all aspects of Medicare Part D benefits administration.. Works closely with all departments necessary to ensure that the processes, programs and services are accomplished in a timely and efficient manner in accordance with CHG policies and procedures and in compliance with applicable state and federal regulations including CMS and/or Medicare Part D, DHCS, DMHC, and applicable accreditation agencies such as NCQA. Works to meet CMS regulatory requirements for Medicare Part D, including but not limited to compliance related to formulary administration, Part D coverage determinations process, Medicare reporting, PDE resolution, Medicare medication safety and overutilization monitoring, and fraud, waste and abuse activities.. Application level understanding of HIPAA, Privacy Act, and ERISA. Frequent traveling, including driving within the County of San Diego.
CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. The Quality and Regulatory Compliance Specialist is responsible for ensuring that development processes for all in vitro diagnostic (IVD) products comply with applicable regulatory requirements and quality standards. Support preparation of internal quality and regulatory documents in support of regulatory submission (De Novo and 510K) for IVD products. 3+ years of experience in regulatory affairs, quality assurance, or compliance within the medical device or In Vitro Diagnostics industry.
Join to apply for the Biostatistician role at Philips. As a Biostatistician, you will conduct advanced statistical analyses to support clinical research studies, ensuring appropriate methodologies are used.. Perform complex statistical programming using software such as SAS or R, generate tables, listings, figures (TLFs), and prepare datasets for regulatory submissions.. You have a bachelor’s degree in Biostatistics or equivalent and 2+ years of experience in areas such as Biostatistics, Clinical Research Study Design, Statistical Programming and Analysis, MedTech, Healthcare Administration or equivalent OR no prior experience required with Master’s Degree.. Get notified about new Biostatistician jobs in San Diego, CA.