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A Travel Nurse RN specializing in Operating Room care, providing direct nursing support during surgical procedures to ensure patient safety and optimal outcomes.. ALOIS Healthcare is seeking a travel nurse RN OR - Operating Room for a travel nursing job in Philadelphia, Pennsylvania.. Operating room nurses provide direct and individualized nursing care to patients based on best-in-class operating procedures, nursing disciplines, and patient safety protocols.. ALOIS means “brave warrior” and that’s what you are- Warrior in Scrubs!. travel nurse, operating room nurse, RN, surgical nursing, patient care, healthcare, perioperative nursing, temporary nursing assignment, clinical coordination, nursing protocols
Join Emory Healthcare (EHC) if you’re looking for an opportunity with one of the nation's leading Atlanta hospitals in cardiology and heart surgery, cancer, neurology, and more!. (No weekends, No Holidays, AOC - 4 week intervals). Emory University Hospital (EUH) is a premier academic medical center within Emory Healthcare (EHC) that serves a high acuity patient population.. We are actively recruiting an Evening Pharmacy Operations Supervisor for the Emory University Hospital (Clifton Rd. campus) Department of Pharmacy.. Emory Healthcare (EHC) , part of Emory University (EUV), is the most comprehensive academic health system in Georgia and the first and only in Georgia with a Magnet® designated ambulatory practice.
The Patient Safety Officer (PSO) is responsible for the development and oversight of the organization’s. The PSO serves as the point of contact and liaison with internal and external stakeholders on patient safety issues. The PSO works to minimize incidents that may impact the safety and wellbeing of patients, staff, contractors, and visitors. Responsible for conducting and coordinating multiple performance improvement functions that foster quality improvement, patient safety, early intervention for potential risk management concerns, and accreditation requirements for the St. Peter’s Health system. Category:Healthcare, Keywords:Patient Safety Specialist, Location:Helena, MT-59604
Location: Greater Boston, MA (Hybrid) | Full-time | Energy / Policy / Regulatory. We are recruiting on behalf of a leading U.S. clean energy company focused on modernizing power generation.. The Manager, External & Regulatory Affairs will help lead the company's engagement in ISO/RTO markets, including PJM, MISO, and SPP. This role is ideal for someone with a strong grasp of power market dynamics and a passion for regulatory strategy and advocacy.. Support regulatory and market strategy across PJM, MISO, SPP, and other emerging U.S. markets. 5+ years' experience in electricity markets, power generation, or regulatory affairs
Under the general supervision of the Director Risk Management, the Patient Safety Manager is responsible for overseeing and implementing systems and processes to ensure the safety of patients. The Patient Safety Manager develops education and works to influence leaders to achieve measurable improvements in patient safety that will support the sustainability of reductions in medical/healthcare errors and other factors that contribute to unintended adverse patient outcomes. A high priority of the Patient Safety Manager is to create a culture of safety within the hospital that prioritizes the well-being of patients and minimizes the risk of harm. Within 30 days of hire: California Fire and Life Safety Card - National Organization.. Within 30 days - California Fire & Safety Card
Emanuel Medical Ctr campus. The nursing philosophy at Legacy focuses on our patients and their families.. The Safety Attendant participates as a member of the healthcare team by assisting the Licensed Independent Practitioner (LIP) and RN. This team member will be responsible for ensuring a safe environment for patients requiring direct or indirect observation.. Training or coursework in behavioral health field preferred.. Keyboard skills and ability to navigate electronic systems applicable to job functions.
Discover why Cooper University Health Care is the employer of choice in South Jersey.. Assists in providing direct, indirect, and non-patient care responsibilities.. Contributes to quality patient care by serving as a significant member of the health care team.. Previous hospital/patient care experience preferred and and/or CNA Certification.. American Heart Association CPR Certified.
Vir Biotechnology is looing for a Regulatory Affairs Manager to join the regulatory group. Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS. Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities.. Pulmonary or respiratory conditions, for example, tuberculosis, asthma, emphysema.. Traumatic brain injury
We believe that blockchain and digital asset innovation will transform how value moves through the world and were building the products and services to make that future a reality. Our institutional digital assets platform spans trading, investment banking, asset management, staking, self-custody, and tokenization technology. Led by CEO and Founder Michael Novogratz, our team blends deep crypto expertise with institutional experience and a shared commitment to shaping the future of Web3 and AI. In addition to ensuring compliance, you will attend Independent System Operator (ISO) or Public Utility Commission (PUC) stakeholder meetings, workshops, and discussions to advocate for Galaxys position within the relevant market. Direct, recent experience within the ERCOT and PUCT stakeholder environment
Arcellx isa public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. Maintain detailed knowledge of global regulatory environment relevant for cell therapies and regenerative medicine. BSc in natural or health sciences (biology, pharmaceutical sciences, or equivalent). Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer.
Mirador is a next-generation precision medicine company focused on immunology and inflammation.. Launched in 2024, Mirador has raised over $400 million from leading life sciences investors and is based inSan Diego, CA.SummaryWe are seeking a motivated individual to join our Regulatory Affairs team and be responsible for leading development and implementation of regulatory CMC strategy primarily for biological assets.. Plan, prepare, author, and / or review CMC-focused content for health authority submissions (e.g., scientific advice briefing packages, CTA, MAA) to health authorities to support clinical trials, registration, maintenance of registration, post-approval registration changes, and / or labeling of pharmaceutical products.. Drive strategy for M3 content for IND / IMPD / CTA and NDA / BLA / MAA in collaboration with CMC and Quality colleagues.. Global Regulatory Affairs CMC experience with biologics.
BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique CELL+GENE platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases. Experience and knowledge of global regulations for the development of cell therapy products is required, and any experience in the neurology and/or ophthalmology therapeutic areas is desired. Represent Regulatory CMC on and/or lead matrix teamsfor cell therapy pipeline products. Minimum Requirements The ideal candidate should have a strong background in Regulatory Affairs CMC in a global pharmaceutical and/or biotechnology company with expertise in biologics, deep experience in product development and understanding of US, international regulations, and ICH guidelines related to biologics and cell therapy development. At least 12-15 years in Regulatory Affairs, CMC, and relevant years in a global pharmaceutical and/or biotechnology company with expertise in biologicals and/or cell and gene therapy products (preferred).
Develop and Execute Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory strategies for Biologics, Biosimilars, and Small Molecules.. Lead and Manage Global Submission Activities: Oversee submission planning, authoring, reviewing, and coordination for regulatory filings (e.g., BLA, MAA).. Assess regulatory impact of changes in CMC procedures and oversee internal regulatory guidance documents.. Master Degree (MS/MA) Science degree (Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) - Required. Substantial knowledge/experience in regulatory submission and approval processes and ability to deal with complex CMC regulatory issues and requirements.
You will be exposed to cutting edge legal and policy topics in the rapidly evolving blockchain and crypto industry, where the story is now being.. Knowledgeable about blockchain technology and the US and Latin America crypto-asset regulatory landscape.. Knowledgeable about US and Latin American financial regulations, such as those applicable to crypto-asset service providers, payment services providers, E-money institutions, banks and custodians, securities and financial instrument issuers, and trading platforms.. Willingness to register as a lobbyist if required.. Regulatory Affairs Director, Emergency Management and Safety Fairfax County, VA $225,000.00-$275,000.00 2 weeks ago
Samaritan Healthcare is seeking a Quality Director for our growing community!. Project Manager Data Analyst, Business Intelligence Analyst, Project Coordinator, Quality/Patient Safety Coordinator, & Infection Preventionist.. Regulatory compliance (DNV, DOH, Stark, etc). Certified Professional in Healthcare Quality (CPHQ) preferred. Extensive experience in curriculum development, instructional design, and program management, preferably in a healthcare or medical education setting.
Work with the Compliance Department to implement new GRC tools related to policies.. Proficiency in Microsoft Word, Excel, and PowerPoint and Governance, Risk & Compliance solutions.. If you need a reasonable accommodation for any part of the employment process, please email our HR Service Center at MyHRHelp@ntrs.com.. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email our HR Service Center or call 1-800-807-0302 (North America), +630-276-5353 (Asia Pacific), 1800-425-0333 (India), +44(0)207 982 4357 (Europe, Middle East and Africa) and let us know the nature of your request and your contact information.. Equal Employment Opportunity Statements APAC/INDIA EEO STATEMENT
NewYork-Presbyterian is one of the nation's most comprehensive academic healthcare delivery systems, dedicated to providing the highest quality, most compassionate care to patients in the New York metropolitan area and throughout the globe.. Lead a World-Class team where you'll channel your superior clinical and business acumen to drive engagement, process improvement, and infection control and prevention.. As the Patient Care Director, you will also manage patient care delivery in the hospitalist units, serving as a clinical resource and administrator in the absence of unit leaders or when care-related issues arise.. 2023 “Workplace Well-being Platinum Winner” – Aetna. “Silver HCM Excellence Award for Learning & Development” – Brandon Hall Group
This is a senior attorney role in the Regulatory Affairs Practice Group, reporting to the Chief Regulatory Counsel.. The Assistant General Counsel also will provide counsel to other areas of the Law Department, including Complaints, Litigation & Investigations, and Cybersecurity when their work presents regulatory issues that benefit from close coordination with the Regulatory Affairs Practice Group.. Provide counsel to other areas of the Law Department, including Complaints, Litigation & Investigations, and Cybersecurity, among others, when their work presents regulatory issues that benefit from close coordination with the Regulatory Affairs Practice Group. Law degree (J.D. or equivalent) and New York bar admission required. This role is based in our Hudson Yards office in New York, NY, 3 days per week, with the ability to work from home 2 days per week.
At T-Mobile, we strongly encourage everyone, including people of color, veterans, military spouses, individuals with disabilities, lesbian, gay, bisexual, transgender, queer and non-binary people, and parents to apply.. And T-Mobile is recognized as a best place to work for LGBTQ employees by the Human Rights Campaign Corporate Equity Index over 10 years in a row.. If your answer is “yes,” you should join T-Mobile’s All-Star Legal Team!. Review FCC filings of T-Mobile and other licensees including entries in the Universal Licensing System and Broadband Data Collection portals.. 2- years of experience as a FCC, DOJ, corporate, or transactional attorney.
Employer Royal Cornwall Hospitals NHS Trust Employer type NHS Site Royal Cornwall Hospital Trust Town Truro Salary Involvement payment with reasonable expenses Closing 27/07/2025 23:59.. You'll be working with the Patient Safety Specialist who is also the Lead for Safety Culture to apply best practice and nurture our teams. Working for our organisation Royal Cornwall Hospitals NHS Trust is the biggest provider of healthcare services in Cornwall and the Isles of Scilly. Enjoy an outstanding quality of life in a place that offers surfing beaches and fishing harbours to beautiful countryside and historic towns. Should you require an alternative format of this application form (such as Braille, audio or large print), please telephone 01872 255755