Collecting information
Organizing data
Cross Country Nurses is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Kingwood, Texas.. As a registered nurse (RN), you will provide care for patients dealing with illness or injury.. Depending on your role, you'll work at a hospital, outpatient center, private practice, home health, telemedicine, nursing facility, clinic or other facility.. You'll perform tasks like assessing patients, developing care plans, administering medication, providing treatment, assisting with surgery, changing bandages, monitoring vitals and maintaining records.. Posted job title: Registered Nurse / Clinical Research RN
Core Medical-Perm is seeking a Registered Nurse (RN) Quality Assurance Director for a nursing job in Las Vegas, Nevada. Job Description & Requirements Specialty: Quality Assurance Discipline: RN Start Date: ASAP Duration: Ongoing 40 hours per week Shift: 8 hours Employment Type: Staff DIRECTOR OF QUALITY $90,000-$120,000 We are looking for a healthcare professional who is ready to provide exceptional patient care in this permanent position. Join other healthcare professionals on the annual Club Coremed retreat and you'll see why candidates choose to work with us to expand their careers. We have jobs nationwide in travel nursing, travel allied health, interim, locum tenens, and permanent placements!. Join the staffing agency with Club CoreMed, the best perk in the industry - an all inclusive paid trip to a tropical resort!
Cross Country Nurses is seeking a travel nurse RN Research / Clinical Research for a travel nursing job in Kingwood, Texas. As a registered nurse (RN), you will provide care for patients dealing with illness or injury. Depending on your role, you'll work at a hospital, outpatient center, private practice, home health, telemedicine, nursing facility, clinic or other facility. You'll perform tasks like assessing patients, developing care plans, administering medication, providing treatment, assisting with surgery, changing bandages, monitoring vitals and maintaining records. Posted job title: Registered Nurse / Clinical Research RN
-Provide medical and clinical expertise into the conduct of clinical trials. Provide leadership and oversight of clinical research staff focusing on patient safety and compliance to study protocols and all regulatory requirements. Evaluate and assesses clinical trial participants to ensure their for enrollment into the clinical trials. Helps to provide supplemental protocol training for staff to ensure a thorough understanding. Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current medical and clinical trial knowledge
The role will identify and engage HCPs and patient advocacy groups through collaborative partnerships to enhance educational initiatives, advance the appropriate application of therapies that provide patient-centric outcomes, and advise the medical and clinical affairs department on matters of strategic importance, including clinical trials.. Lead the planning and operations of the Santreva Podium & Publication (PnP) Committee, aligning cross-functional teams to deliver high-impact scientific projects.. Provide scientific and clinical insights to support the development and execution of clinical trials, publications, and medical education programs.. Advanced degree (MD, PhD, or PharmD) in a relevant scientific discipline.. Clinical research experience in medical devices, biologics, or drugs is strongly preferred.
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.. 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). Instructional Designer, Collision RepairInteractive Media and Instructional DesignerMicro-learning Designer and Video Producer (Hybrid role) - ContractorDirector of Technical Training DevelopmentSpanish Language Arts Curriculum Designer
Reporting to the VP and Head of Legal, US, the Assistant General Counsel (AGC), US Prescription Business Unit will be located either in Galdermas Boston office in a hybrid (3 days in office) environment, or remote with a requirement to travel ~2-5 times per year for meetings. The successful candidate will have a minimum of 7 years of legal experience as a healthcare attorney advising on US Market Access/Reimbursement, managed care and patient services in a law firm, payer or pharmaceutical manufacturer environment, with some level of in-house experience preferred. Draft, negotiate and review commercial agreements, including PBM, GPO, Medicare/Medicaid, payer, formulary, specialty pharmacy, wholesaler, discount and rebate, distribution, vendor and supplier contracts related to reimbursed prescription products for the treatment of various dermatological skin conditions. Juris Doctor (J.D.) degree from an accredited U.S. law school required. At least 7 years of legal experience as a healthcare attorney advising on US Market Access and patient services in a law firm, payer or pharmaceutical manufacturer with some level of in-house experience preferred
Sales Team will be led by Chief Experience Officer with over 20 years of C- level, GM, and Business Development experience in Medical Devices, AI, System Technology and Pharmaceuticals, including 6+ years of entrepreneurship.. Led Quality Assurance and Regulatory affairs activities for 5 new product development and 10 product sustenance programs. Hands on experience in 510K and PMA submissions. Experience in Business strategy, Regulatory, Quality, R&D and Product strategies, managed regulatory concept and quality assurance: feasibility, requirements, usability, integration, testing/automation, verification, reliability, security, validation, post market quality.. Strong team building skills, strategy, and operations thinking, solution & result orientation.
This position is responsible for handling of Controlled Substance related activities and QMS.. Maintaining Deviations, Investigations, CAPA, Change Controls, Protocols Trackers-Logbooks.. Issuance, Retrieval and Archival of Logbooks. Carrying out Quality Inspection of all incoming batches per current approved procedure. Minimum 1 to 5 years of related experience in the pharmaceutical industry, handling controlled substance, QMS, Warehouse compliance and Inspection activity.
The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials. At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
The Billing/AR Specialist at Applied Behavior Center for Autism is responsible for managing the organization's accounts receivable processes, ensuring accurate and timely collection of payments from clients, insurance companies, and other stakeholders.. The ideal candidate will have a strong understanding of health insurance, experience in healthcare or medical billing, and a passion for contributing to the growth and success of a center dedicated to helping children with autism.. o Track and log denials, appeals and claim follow-ups using the appropriate systems. o Assist with insurance verification and pre-authorizations to ensure services are covered before treatment begins. Experience Required: Minimum of 2 years' experience in a healthcare or medical billing environment required.
+ Minimum of 3 years of direct patient care experience, including 2 years in a hospice or home-based care setting. + Minimum of 3 years of direct patient care experience, including 2 years in a hospice or home-based care setting.. Demonstrated ability to apply hospice principles, industry standards, and regulatory compliance (Medicare, Medicaid, JCAHO, ACHC).. Wellness Programs (Telemedicine, Diabetes Management, Joint & Spine Concierge Care).. Education Support & Tuition Assistance (ASN to BSN, BSN to MSN)
Quality Assurance Analyst supports Data Management development at Rush Health, a clinically integrated network of physicians and hospitals working together to improve health through high-quality, efficient health services covering the spectrum of patient care from wellness, prevention and health promotion, to disease management and complex care management.. Our network includes Rush University Medical Center, Rush Oak Park Hospital, Rush Copley Medical Center, Riverside Medical Center, and over 2000 physician members and 250 non-physician network clinicians.. Provide feedback on data quality (to the RHA Data Sourcing team, as well as to source entities) and regularly evaluate the impact of data quality issues on the end reports and end users.. This will include using master data appropriately in reporting and analytical tool development; documenting master data rules as they relate to reporting needs; working with data stewards to profile and correct master data; and developing user tools to support master data management. QA Tester / Contract To Hire / Hybrid / South Suburbs of Chicago
Provide leadership, project management, direction, and program oversight to plan and conduct high-quality clinical trial protocols according to the specified clinical protocol, Good Clinical Practices (GCP), and FDA regulations.. Actively oversee Pharmacovigilance activities in collaboration with clinical teams, including real-time medical monitoring of clinical trials.. Responsibilities include assessing patient eligibility, addressing study design inquiries, and responding to urgent safety concerns to ensure patient safety, regulatory compliance, and efficient communication of drug safety information to clinical teams and senior management.. Work closely with cross-functional teams, including clinical operations, data management, statistics, regulatory affairs, biomarker scientists, and information technology (IT), to ensure effective coordination and seamless collaboration.. Working knowledge of global PV requirements (e.g., US Code of Federal (CFR) regulations; European Union (EU); Guideline on Good Pharmacovigilance Practices (GVP) and ICH guidelines.
At Priority Life Care (PLC), we provide you the opportunity to use your talents in a progressive, growing organization that makes a positive difference in the lives of the seniors we serve.. SwiftMD Telemedicine, at low or no cost!. No need to wait until payday!. Must be licensed in the applicable state as a Licensed Practical Nurse (LPN). Experience with the applicable state Survey Rules & Regulations, Medicare and Medicaid
Supervise training in other laws such as the Physician Payment Sunshine Act, HIPAA, Stark Laws, and related.. Billing and coding, privacy and security, credentialing, and MMHS contracting; managed care.. Laws relating to Medicare, Medicaid, EMTALA, HIPAA, the Stark Law, the False Claims Act, and the.. Knowledge of Managed care systems of a Knox-Keene licensed health.. Certified Professional in Healthcare Quality (CPHQ), or Healthcare Quality and
Assists the hospital and medical-staff leadership in meeting The Joint Commission and CMS Standards as well as other state and federal regulatory requirements, complying with corporate policies and procedures. Responsible to provide comprehensive assessment, planning, monitoring, and evaluation for compliance with accreditation and regulatory agencies including any state licensing standards. The Director is responsible for directing and coordinating regulatory and accreditation functions, ensuring appropriate preparation, and active participation of appropriate staff and managers for agencies such as The Joint Commission (TJC), Florida's Agency for Healthcare Administration (AHCA), and/or the Centers for Medicare and Medicaid Services (CMS) and to formulate responses to accreditation findings and inquiries. Facilitates, develops, and implement special projects as assigned by the VPQ and CMO. Develop audit systems, perform data analysis and prepare reports related to measuring objectives and tracking outcomes. CPHQ (Certified Professional in Healthcare Quality) OR CHCQM (Diplomate in American Board of Quality Assurance and Utilization Review Physicians)
Medical Science Liaison (MSL), Medical Affairs - North Central Join to apply for the Medical Science Liaison (MSL), Medical Affairs - North Central role at Madrigal Pharmaceuticals.. Advanced degree in healthcare or science-related area of study (e.g., MD/DO, PharmD, PhD, DNP, PC) or other life sciences or equivalent with solid medical/technical background. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Senior Medical Writer (Contract-to-Hire) Principal Medical Writer (Contract-to-Hire) Sr. Program Manager, Medical Affairs (Heathcare Systems Partnerships) Director of Regulatory Affairs - Medical Devices Minneapolis, MN $185,000.00-$225,000.00 1 week ago.. Medical Science Liaison, Rheumatology - CO, MN, OK, NE, SD, & ND Minneapolis, MN $115,000.00-$197,850.00 1 week ago
Join to apply for the Associate Director, Medical Writer role at MannKind Corporation. Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.. Minimum of 5 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R&D.. Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.. Sweetwater Veterinary Clinic - Medical DirectorAssociate Director to Director, Statistical Programming
The incumbent might also be designated as U.S. Agent (back-up) for the U.S. Office for both ANDAs (GPI USA) and API (GLS India).. Support the U.S. Office for more than 170 approved ANDAs and all unapproved (under review ANDAs) as U.S. Agent back-up for all Glenmark subsidiaries including GPL, GSSA, GPI and GLS. The successful candidate will need to be able to review and sign various submissions to FDA. It will include ANDA cover letter, Form 356H for Original ANDAs, Amendments to ANDAs and/or Supplements to post-approval work.. The email list is provided for such communications which includes Commercial Division Heads, R&D, QA, Legal, Business Development, Project Management, Demand Planning, Marketing and others identified on the list.. Separate communications received from the FDA to support GLS will be sent to the GLS leadership team as identified.. B.S. in Chemistry or Biology, or Engineering degree in Biotechnology or Chemical Engineering