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Quality Assurance Manager (Hybrid Remote in Richmond, VA). Maximus is hiring a Quality Assurance Manager who will play a critical leadership role in ensuring the integrity, effectiveness, and continuous improvement of the Quality Assurance program.. Comprehensive Insurance Coverage: Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance.. Holistic Wellness Support: Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP).. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances.
This position works closely with key stake holders including Clinical Operations, Global Planning, Quality Assurance, Regulatory Affairs, Contract Manufacturing Operations (CMO’s), and Contract Research Operations (CRO’s) to ensure seamless supply of Clinical Trial Material.. Some key areas of management/oversight include forecasting, packaging, labeling, distribution, inventory management, financial planning/ budgeting, vendor oversight, and eTMF filing of Clinical Supply documents.. Managing packaging, labeling, and distribution of clinical trial material for global clinical trials. Support (Interactive Response Technology) IRT development, user acceptance testing (UAT), and system oversight, as well as utilize the system to actively manage clinical trial material.. NSIDE, Bioclinica, 4G, Oracle, etc)
The Intake Patient Care Representative is responsible for admitting new patients, verifying insurance information, and completing all applicable admissions paperwork.. Candidates in the Central or Eastern time zones will be prioritized for consideration.. Various clerical work including faxing, scanning, and copying. Experience in healthcare preferred; knowledge of insurances and respiratory care is a plus. 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.
Working knowledge of biologics drug development, clinical research, study design, biostatistics, regulatory, and medical terminology.. Computer proficiency in Microsoft Office (including Word, Excel, PowerPoint, and Project Management tools) with some experience with Veeva Vault products and MW artificial intelligence (AI) software/writing tools would be a g plus.. Head (Executive Director) Rare Disease, US Medical Affairs. Medical Director, Drug Safety & Pharmacovigilance. Senior Medical Director, Drug Safety & Pharmacovigilance
Our innovative approach to health insurance shopping and enrollment has expanded beyond exchanges, and we’re now reinventing the way states administer safety net programs such as Medicaid, SNAP (food stamps), child care, and unemployment insurance.. Prior work with public sector or HHS programs (SNAP, TANF, Medicaid) is strongly preferred/. Exposure to Genesys, NICE, or other contact center platforms.. Quality Assurance Specialist, Financial Crimes. $29/hr - Autonomous Vehicle Operator (Testing and Quality Control)
The Insurance Patient Account Representative is an extension of a client’s business office staff.. Ability to initiate and follow through on projects and work independently with minimal supervision. #Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.. ~ Tuition Reimbursement, Personal Development & Learning Opportunities. ~ Corporate Sponsored Events & Community Outreach
The Regulatory Affairs Director (RAD), Global Regulatory Strategy, will be responsible for the development and implementation of global regulatory strategies for all assigned products and therapeutic areas.. Contribute to internal governance and advisory bodies for strategic and operational insights.. Collaborate with senior management and enterprise functions to provide regulatory insights and drug development expertise.. Strong knowledge of drug development, regulatory policy, and scientific and business judgment.. Bachelor’s Degree in life sciences or related field; postgraduate degrees (MSc, PhD) are a plus.
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.. Family support through fertility and family building benefits with Progyny and adoption assistance.. Referral services for child, elder and pet care, home and auto repair, event planning and more. The Patient Safety Attendant (PSA) participates in high-quality, patient-centered care by providing continuous observation and monitoring for high risk patients.. HCA Healthcare Co-Founder
Provide internal and external consultancy on safety issues related to Pharmacovigilance and Patient Safety activities (processing safety and epidemiology reports, providing benefit-risk assessments, signal detection and investigations). Act as an expert to department and organization members regarding risk management, insurance, legal and regulatory matters. MD or an advanced degree in Pharmacy or Health Sciences (PharmD, PhD). Extensive professional experience in pharmacovigilance and clinical safety and understanding of clinical research development. Experience in clinical trials from CRO or pharma/biotech company or as an investigator
Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.. Family support through fertility and family building benefits with Progyny and adoption assistance.. Referral services for child, elder and pet care, home and auto repair, event planning and more. The Patient Safety Attendant (PSA) participates in high-quality, patient-centered care by providing continuous observation and monitoring for high risk patients.
Clinical Research Associate I Job at Abbott, Alameda, CA Abbott. Job Description Abbott is a global healthcare leader dedicated to helping people live more fully at all stages of life.. Bachelor's degree in life sciences preferred, with two years of experience as CRC/CTA or equivalent. Knowledge of GCP, Clinical, and Regulatory Affairs is a plus. Abbott is an Equal Opportunity Employer committed to diversity and inclusion.
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.. Family support through fertility and family building benefits with Progyny and adoption assistance.. Referral services for child, elder and pet care, home and auto repair, event planning and more. CJW Medical Center is comprised of Chippenham Hospital and Johnston-Willis Hospital.. HCA Healthcare Co-Founder
The Director of Biomedical Engineering (Healthcare Technology Management) is responsible for leading and overseeing the strategic planning, implementation and maintenance of biomedical equipment and systems including biomedical engineering initiatives.. Compliance & Safety: Ensure adherence to regulatory standards, such as FDA, HIPAA, Joint Commission and Cybersecurity to maintain patient safety and data security.. Vendor & Stakeholder Relations: Collaborate with medical device manufacturers, HTM/IT vendors, healthcare administrators, and clinical teams to streamline technology solutions.. Education: Bachelor of Science in Biomedical Engineering, HTM, IT or a healthcare field required.. Five years' management in a healthcare IT or Biomed/HTM environment required.
Certified Professional in Healthcare Quality (CPHQ), or Healthcare Quality and Management Certification (HCQM), or Certificate of Professional Healthcare Quality and Patient Safety (CPQPS) within two (2) years of employment is required.. Founded in 1887 Dignity Health - California Hospital Medical Center is a 392-bed acute care nonprofit hospital located in downtown Los Angeles.. Quality & Safety Improvement Consultant IV, Clinical Quality Consulting (PMG) Quality & Safety Improvement Consultant IV, Patient Safety (KFH/HP) Quality & Safety Improvement Consultant IV, Clinical Quality Consulting (KFH/HP) Los Angeles, CA $96,200.00-$128,300.00 4 weeks ago. Quality & Safety Improvement Consultant IV, Clinical Quality Consulting (KFH/HP) Quality Assurance Manager - Aerospace / Manufacturing Monterey Park, CA $85,000.00-$110,000.00 2 weeks ago. Manager, Quality Assurance (H/F) - MAG AEROSPACE INDUSTRIES, LLC Quality Patient Safety Program Manager Licensed Quality & Safety Improvement Consultant IV, Clinical Quality Consulting (PMG) Sr. Manager, Quality & Mission Assurance We’re unlocking community knowledge in a new way.
Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens. Certification as a Clinical Research Associate or Coordinator. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care.
The main responsibilities include supporting clinical evidence generation, collaborating with cross-functional teams for co-developing companion diagnostics in oncology, and supporting clinical trial design, regulatory applications, and scientific marketing.. The ideal candidate will have a strong background in clinical science or research, with experience in pharmaceutical, biomarker, or in vitro diagnostic clinical development.. You will work closely with pharmaceutical partners, R&D scientists, Clinical Trial Managers/Clinical Research Associates, Quality Assurance, and Regulatory Affairs to ensure compliance with internal and external standards.. Contributing to cutoff/cutpoint determination, method comparison, bridging, and analytical concordance studies.. Knowledge of clinical trial design, conduct, oversight, biostatistics, and GCP.
We are looking for a clinical researcher to join our team to train AI models.. In this role you will need to hold an expert understanding of clinical research topics- a completed or in progress Masters/PhD is preferred but not required.. Other related fields include, but are not limited to: Epidemiology, Biostatistics, Regulatory Affairs, Medical Ethics, Clinical Pharmacology, Health Economics, Translational Medicine, Nursing, Public Health.. A current, in progress, or completed Masters and/or PhD is preferred but not required. Note: Payment is made via PayPal. We will never ask for any money from you.
DescriptionKEY RESPONSIBILITIES: Functions as an expert research nurse or coordinates a multi-center trial.. Provides leadership and expertise in identifying and writing research grants, publications in medical and nursing literature, study materials, brochures and correspondence.. Along with Principal Investigator, may represent a study at Patient Safety Monitoring Board meetings at the NIH. Regularly functions as a preceptor or mentor.. Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.. Must be credentialed through Emory Healthcare in RN II : Position tasks are required to be performed in-person at an Emory University location; working remote is not an option.
The Clinical Research Coordinator II RN (CRC-II RN) serves the AdventHealth Research Institute (AHRI), under limited supervision, to plan, coordinate, evaluate and perform the nursing care of participants and collect data for assigned research projects.. The CRC-II RN works to advocate for the patient, while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines.. Serves as liaison between Principal Investigators and the Institutional Review Board (IRB) and the Office of Sponsored Programs (OSP).. Prepares and/or reviews all required documentation for clinical research study start up, execution, modification, renewal, and termination and will meet all reasonable deadlines for submission.. Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA
To achieve service quality, the Clinical Research Coordinator Supervisor will work closely with staff to identify areas in need of training and development, review, and refreshers.. 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.. 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.