Collecting information
Organizing data
Additionally, the Patient Care Technician may assume the responsibilities of a health unit coordinator.. May assume the responsibilities of a health unit coordinator, including answering phones, transcribing physician orders, managing unit records, organizing, stocking, and maintaining unit supplies.. St. Marys Regional Hospital. We care about your well-being – mind, body, and spirit – which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.. At Intermountain Health, we use the artificial intelligence ("AI") platform, HiredScore to improve your job application experience.
Medical Oncologist - GI Malignancy Program Leader Location: Charlotte, NC We are seeking a board-certified or board-eligible Medical Oncologist to lead our GI Malignancy program in Charlotte, NC. This is an exciting leadership opportunity in a growing cancer program committed to excellence in patient care, research, and innovation.. Work in a state-of-the-art, multi-million-dollar Cancer Institute facility in uptown Charlotte.. Collaborate with colorectal surgery, hepatobiliary surgery, radiation oncology, and other GI-specific subspecialists.. Strong interest in clinical research, with experience in early-phase clinical trials preferred.. Enjoy world-class dining, cultural attractions, professional sports, and green spaces like Freedom Park and the Carolina Thread Trail.
Compensation : Base salary up to $220k, Plus Bonus, Plus LTI. Scientific Search has recently partnered with an innovative biopharmaceutical company who has tasked us in finding them a Director, Regulatory Affairs. Support European development-stage regulatory activities, including contribution to CTA and MAA strategies and filings (execution will be led by regional team). Bachelor’s degree in life sciences required; advanced degree (MS, PharmD, PhD, or equivalent) strongly preferred.. Prior involvement in European regulatory strategy and filings (e.g., CTA, MAA) preferred
Director of Research - Hematology/Oncology Opening in MA Located in Burlington & Peabody, MA Full-Time & PermanentSeeking a BE/BC Hematologist/Oncologist to join group as the Director of Research.. Lead Clinical Research: Oversee research operations at facilities in Beverly, Addison Gilbert, Anna Jaques, Winchester.. Educate & Mentor: Train medical students (UMass Chan School of Medicine) and fellows in our new hematology-oncology fellowship program.. State-of-the-art facilities with infusion, radiation oncology, genetics, and molecular diagnostics.. Competitive salary and comprehensive benefits package: 4 weeks vacation, 10 holidays, 20 CME days Licenses, board exams, liability coverage Health, dental, and vision insurance 403B and 457B retirement plansLocation:Burlington, MA is a scenic suburban community approximately 17 miles northwest of Boston and a short drive to the lakes, mountains, and shores of New England.
Community Hospital is hiring a PRN Patient Care Tech for Pain and GI!. Under the supervision of a registered nurse, the Patient Care Tech performs delegated direct patient care activities to an assigned group of patients.. Performs a variety of tasks including phlebotomy, electrocardiogram, cleaning of care areas, stocking, disposal of linen and supply materials to ensure assigned areas are kept clean and adequately supplied.. Completion of a nursing assistant (CNA, MA, AUA) training program or equivalent OR. Must have one year clinical hospital experience as a PCT/CNA/MA and formalized phlebotomy, order entry and EKG/Dysrhythmia Interpretation training OR AUA certification and completion of a formalized phlebotomy, order entry and EKG/Dysrhythmia Interpretation training OR Completion of two semesters of clinical nursing courses in an accredited RN program and competency completion in phlebotomy, order entry, and EKG/Dysrhythmia Interpretation
From cellular phones to lower emission vehicles, to 5G communications and clean energy from hydrogen, we're collaborating with customers to make these innovations more capable.. Chemours is seeking a Director of Regulatory Advocacy to join our growing Government Affairs team!. The successful candidate will join Chemours' Global Government Affairs Group with a primary responsibility for supporting U.S. federal regulatory affairs engagement with the United States Environmental Protection Agency (USEPA), as well as other select federal administrative agencies; key trade organizations that help shape regulatory policies at the U.S. federal level; and members of the U.S. Congress and their staffs.. Liaise with the Chemours' businesses, as well as corporate functions such as Legal, Corporate Remediation, Environmental Center of Excellence, Corporate Sustainability, Corporate Product Regulatory Compliance, Corporate Toxicology and Risk Assessment, and Communications, among others, to ensure coordination and integration of the company's public policy agenda.. Immigration sponsorship (i.e., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant status) is not currently available for this position
At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock.. Lead Correspondence with US Agencies (CVB-IC and FD-ORA). Maintain current registrations with the US Drug Enforcement Administration. Biological/Chemistry based degree: B.S. with 14 years, M.S. with 12 years, or DVM/Ph. D. with 9 years, with direct experience in biological or pharmaceutical science development or manufacture.. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock.
The Principal Regulatory Affairs Specialist provides regulatory leadership for product manufactured by PROCEPT BioRobotics (“company”) from development through marketing approval and commercialization.. The initial role of the Principal Regulatory Affairs Specialist will be as an individual contributor, reports to the Senior Director of Global Regulatory Affairs.. Knowledge of EU MDR regulations is required. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept’s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.. We offer a comprehensive benefits package that includes full medical coverage, wellness programs, on-site gym, a 401(k) plan with employer match, short-term and long-term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and many more!
The Regulatory Affairs Program Manager is responsible for a multitude of multi-year projects and programs leading mandatory and strategic regulatory change supporting multiple lines of business. Works closely with Regulatory Affairs Managers to ensure business unit account remediation projects meet regulatory expectations, have effective project plans, and provide regular reporting to Bank executives and the Board. The position reports to the Executive Director of Regulatory Affairs. Work closely with Regulatory Affairs Analyst and business unit subject matter experts and stakeholders to ensure remediation efforts are well planned and effectively executed. Assist Regulatory Affairs management regulatory change management functions to ensure the bank is managing effectively changing regulatory landscape.
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.
We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.. Founded in 2009 from the University of Minnesota's breakthrough advances in perfusion decellularization and recellularization technology, we are the world leader in the research and development of fully biologic organs.. We are focused on the research and development of transplantable kidneys ( mirokidney ), livers ( miroliver ), and a bioengineered external liver assist device for acute liver failure ( miroliver ELAP ), with plans to also bioengineer other critical organs like lungs, pancreases and hearts.. We are looking for a regulatory strategist who will advise on regulatory pathways, managing documentation and timelines, and supporting the preparation and execution of regulatory submissions for our whole organ tissue engineering program.. Must have written an IND and submitted it in ECTD format through the ESG portal
Presbyterian Medical Group seeks a Board Eligible / Board Certified Urologist to join our established practice in Albuquerque, New Mexico.. About Presbyterian Healthcare Services. Presbyterian Healthcare Services exists to improve the health of patients, members and the communities we serve.. With over 300 days of sunshine annually, indulge in outdoor activities ranging from hiking the Sandia Mountains to skiing in nearby Taos.. Remote Telemedicine Physician Men's Hormone Specialist (MD/DO)
Visterra is seeking a Regulatory Affairs professional experienced in biologics development to lead our Regulatory Team's strategy and oversee the team's activities from IND-enabling studies and first-in-human (FIH) studies through clinical proof of concept (PoC) trials, and to facilitate post-PoC transitioning to our Otsuka affiliate for global clinical development & commercialization.. Effectively negotiate alignment with Otsuka parent and affiliate organizations on strategy & messaging to produce optimal outcomes from global health authority interactions.. Define and oversee phase-appropriate CMC regulatory strategy for biologics, including CMC regulatory-specific risk mitigation, and ensuring seamless progression from discovery through early clinical development.. Support CMC functions (e.g. Process Development, Analytical Development, Manufacturing and Quality Control) pertaining to the preparation and content of CTA/IMPDs, PPQs, INDs dossiers to ensure timely delivery of final documents to be included in submissions.. 15+ years of global regulatory affairs experience, including at least 5 - 7 years in biologics, with expertise in early-stage development (IND-enabling, FIH, PoC), CMC regulatory strategy, and global compliance.
Northwest Medical Specialties, PLLC, is a leading Hematology/Oncology practice seeking a motivated, energetic, and compassionate physician to join our team.. The NWMS Hematologist/Oncologist specializes in the diagnosis, treatment, and management of both solid tumors and hematologic malignancies, including leukemia, lymphoma, myeloma, and other hematologic malignancies.. Working in a multidisciplinary healthcare environment, this physician provides expert care to patients, utilizing advanced diagnostic techniques, chemotherapy, immunotherapy, cellular therapy, and stem cell transplantation.. We are specifically seeking a candidate with expertise and or interest in cellular therapy, bispecifics, and CAR-T cell therapy.. Additionally, the hematologist/oncologist plays a critical role in educating patients and their families about disease management, treatment options, and expected outcomes.
Job Title: Regulatory Affairs Associate Director. Job Summary: As Regulatory Affairs Associate Director, you will lead RA team members involved in device project activities and new product development within the Advanced Drug Development Delivery platform.. Associates are required to be onsite at our Franklin Lakes, NJ headquarters Monday through Thursday, with optional work from home on Fridays.. Manage promotional material reviews and ensure external communications align with regulatory requirements.. Educate and train cross-functional teams on EU and FDA regulatory requirements pertinent to pharmaceutical systems and customers.
Partner cross-functionally with Compliance, Legal, Risk, and Corporate Affairs to address emerging trends and advocate for Chimes regulatory positions.. Our in-office work policy is designed to keep you connected - with four days a week in the office and Fridays from home for those near one of our offices, plus team and company-wide events depending on location.. Whether youre coming in regularly or are part of our fully remote program, youll stay engaged with your work and teammates.. Access to Maven, a family planning tool, with $15k lifetime reimbursement for egg freezing, fertility treatments, adoption, and more.. We will also consider qualified applicants with criminal histories in a manner consistent with the requirements of state and local laws, including the San Francisco Fair Chance Ordinance, Cook County Ordinance, NYC Fair Chance Act, and the LA City Fair Chance Ordinance, and consistent with Canadian provincial and federal laws.
Maintain regulatory files for each ingredient (TDS, SDS, Cof A, ingredient breakdown, Impurities profile etc. Support ISO and CGMP quality systems in coordination with global network of corporate regulatory and quality management.. BA/BS in Science; preferably Chemistry, Biochemistry or Microbiology. Health Savings Account (HSA) (for employees working 20+ hours per week). For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Sr. Regulatory Affairs Specialist. A leading designer, developer, manufacturer, and marketer of innovative medical devices used in spinal surgical procedures, Spinal Elements combines leading medical device technologies, biologics, and instrumentation to create positive surgical outcomes that exceed surgeon and patient expectations.. The Senior Regulatory Affairs Specialist is a key member of the Regulatory Affairs team and reports to the Associate Director, Regulatory Affairs.. Additionally, the team works closely with cross-functional departments to support product development, submissions, and post-market surveillance activities.. The Senior Regulatory Specialist is responsible for the coordination and preparation of document packages for regulatory submissions for new and mature products, ensuring alignment and compliance with local, regional, and global registration requirements, as well as company policies.
Embassy of Lebanon has a full-time LPN position available waiting just for YOU with limited PRN left!. Must be able to interpret existing policies and procedures to nursing assistants, restorative nursing assistants, residents, families, and physicians.. Must conduct resident rounds daily, reporting problems to nursing supervisor and initiating corrective action.. Here at Embassy of Lebanon, we are part of a resident-focused team.. Knowledge of EHR systems and HIPAA regulations
As an AE, you will be responsible for owning the full sales cycle for mid-market and growth accounts, with a focus on building relationships across Quality, Regulatory Affairs, and Post-Market Surveillance teams.. You’re a consultative seller with deep curiosity about your customer’s business and a track record of success in complex sales environments.. Top pharmaceutical companies, food manufacturers, medtech companies, and service firms from around the globe rely on Redica Systems to mine and process government inspection, enforcement, and registration data.. This enables them to quantify risk signals from their suppliers, identify market opportunities, benchmark against peers, and prepare for the latest inspection trends.. Our data and analytics have been cited by major media outlets including MSNBC, The Wall Street Journal (WSJ), and The Boston Globe.