Collecting information
Organizing data
At National Staffing Solutions, we have the privilege and honor of working with dedicated healthcare professionals that make a positive impact in aiding those needing healthcare services across the U.S. every day. Perform the initial assessment of the patient and actively participate in all aspects of patient care, including history and physical, diagnostic and therapeutic planning, procedures, writing orders, and interactions with family. Payer mix - 35% Medicare, 15% Medicaid, 35% Commercial, balance is "other".. Age distribution - pediatric to geriatric, high elderly population in area.. Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) degree from an accredited medical school.
The professional registered nurse is knowledgeable of current trends in healthcare including but not limited to advances in technology, pharmacology, treatment care modalities, quality and patient safety.. The professional registered nurse serves as a patient and family advocate while facilitating a cooperative and collaborative environment among all health care providers.. Performs procedures (including IV therapy) and treatments (including nutrition) using nursing knowledge and judgment, according to established unit/practice area guidelines and professional standards. Knowledge and application of the nursing process to implement a nu r sing plan of care.. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, Care at Home - an expansive home care network, and large integrated physician network.
These include, but are not limited to, direct patient care activities such as taking vital signs and assisting patients with the basic activities of daily living, as well as non-clinical activities such as acting as a receptionist, coordinating equipment, providing transportation activities, and performing tasks specific to the department assigned.. The Patient Care Assistant II interacts with patients, families, nursing, and a variety of interdisciplinary personnel and possesses strong interpersonal and communication skills.. The PCA II staff collaborate among themselves to ensure safe patient care and smooth unit operations.. EEO Statement Newton-Wellesley Hospital is an Equal Opportunity Employer.. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law.
Publicly Traded Biopharmaceutical company in Watertown, MA is expanding for their high profile clinical development trials.. The Director, Clinical Operations is a leadership role responsible for overseeing and managing all aspects of clinical operations for a high priority immunology program.. This individual possesses clinical operations expertise with a track record of success, working with peers and stakeholders across multiple disciplines to drive programs with multiple studies and indications through all phases of clinical trials (Phase I-III).. The Director will be a leader in the organization who knows how to manage a team internally, at our clinical sites, and with our vendors.
Join our passionate team and play a crucial role in identifying, attracting, and hiring top talent across a variety of engineering skillsets including, but not limited to, software engineering, embedded application engineering, device testing, and more to support our diverse practice areas.. Create an overall positive candidate experience while engaging with professionals in clinical research, regulatory affairs, pharmacovigilance, quality assurance, and related areas.. Influence hiring decisions through data-backed insights and market intelligence.. Comfortable presenting recruitment data and insights to leadership to drive continuous improvement and strategic alignment.. Sound knowledge of employment laws and regulations, including those relevant to the pharmaceutical and biotech sectors.
BrightStar Care is Seeking a Director of Nursing: Lead with Excellence and Compassion. BrightStar Care, a premier provider of home health care services, is seeking a Director of Nursing to guide and enhance our nursing practices to work on part time or full time basis.. Leadership in Home Health: We are one of the leaders in Home Health Care and are committed to the highest standards of patient care and clinical excellence.. As the Director of Nursing at BrightStar Care, you will play a critical role in shaping our clinical services and enhancing patient outcomes.. We look forward to welcoming a dedicated professional like you to our team at BrightStar Care!
The ideal candidate will support early and late-stage clinical drug development across therapeutic areas by leveraging Quantitative Systems Pharmacology (QSP) modeling to de-risk and optimize development from First-in-Human (FIH) through Proof-of-Concept (PoC) and beyond.. Ph. D. in Engineering, Mathematics, Bioinformatics, Pharmacometrics, Systems Biology/Pharmacology, or a related field. 5+ years of relevant modeling and simulation experience in pharmaceutical R&D or consulting; postdoctoral experience may be considered. Proficiency in general programming and data analysis using tools such as Python, R, MATLAB. Working knowledge of drug development processes and disciplines such as clinical pharmacology, biopharmaceutics, bioanalytics, and toxicologyFor Sr Research Investigator level, the starting compensation for this job is a range from $160,000-$190,000, plus incentive cash and stock opportunities (based on eligibility).
Job Title: MDS CoordinatorLocation: Maplewood Rehabilitation and Nursing Center – Amesbury, MASalary Range: $100,000 to $125,000. MDS Coordinator Position Summary:We are seeking a detail-oriented and experienced MDS Coordinator to oversee and manage the completion and submission of the Minimum Data Set (MDS) in accordance with federal and state regulations.. The MDS Coordinator will play a key role in care planning and reimbursement processes and ensure accuracy and compliance in all resident assessments.. Serve as a clinical resource and mentor to nursing staff related to MDS processes. Prior experience as an MDS Coordinator in a skilled nursing facility (Preferred)
The Senior Specialist, Pharmacovigilance (PV) Quality and Compliance encompasses a key leadership role in providing direction to the PV department and promote the spirit of proactive, continuous quality improvement in adverse event case management for all Deciphera Pharmaceuticals Clinical Trials, Extended Access Programs and post marketing (where applicable). This position will report to the Senior Manager, Pharmacovigilance (PV) Quality and Compliance and be remote or near the Waltham, MA office. Assist in managing vendor and business partner oversight by supporting audit follow-ups, tracking CAPA implementation, and ensuring appropriate documentation. Minimum of 3+ years of experience in Pharmacovigilance (PV) operations and/or quality roles within the pharmaceutical, biotech, or healthcare industry. Hands-on experience with safety databases (e.g., Argus) for case management and regulatory reporting.
Review and provide feedback on CDM and study documents, including the Data Management Plan, study protocols, data transfer agreements, and data validation specifications. Oversee the electronic data capture (EDC) database build process, including review of specifications, data validation documents, and user acceptance testing (UAT) during initial build and subsequent modifications. Collaborate with Programming, Biostatistics, Clinical Operations, Patient Safety, Pharmacovigilance, Medical Science, and other teams to meet project timelines. At least 8 years of clinical data management experience in biotech or pharma, with a strong understanding of late-phase drug development, preferably in Phase 3 Oncology trials. Knowledge of clinical research regulations, including FDA, ICH, GCP, and GCDMP.
Review and provide feedback to CDM and study documents, including but not limited to the Data Management Plan, study protocols, data transfer agreements and data validation specifications.. Oversee electronic data capture (EDC) database build process, including but not limited to review of specification and data validations documents and user acceptance testing (UAT) of the EDC during initial build and subsequent database modification.. Collaborate with Programming, Biostatistics, Clinical Operations, Patient Safety and Pharmacovigilance, Medical Science, and other cross-functional teams to meet project deliverables and timelines.. 8+ years of Clinical Data Management experience in biotechnology or pharmaceutical industry with excellent understanding of late phase clinical drug development processes required.. trong knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements.
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience.. The Senior Director, Biostatistics will be working in a cross functional team, responsible for providing program and project-level statistical expertise and leadership in the development of Ipsen Rare Disease assets.. In addition, she/he will have the capacity to understand relevant multi-disciplinary knowledge and interact effectively with within the biometrics department with clinicians, regulatory affairs, medical writing, clinical operations, service/technology providers, as well data management and statistical programming.. Strong knowledge of SAS programming concepts and techniques in the pharmaceutical, with the ability to proactively address strategic limitations; proficiency in tools such as SAS, R, EAST, nQuery, and JMP.. Rare disease drug development experience is highly desired.
-Developing and managing strong alliances with the Oncology Research, medical affairs, commercial and business development organizations to enable end-to-end execution.. Provide guidance on criteria for clinical candidate selection, guidance during the pre-candidate nomination period and during development to ensure ongoing clinical stage programs are supported by Oncology Research and by Early Development and Translational Sciences as required.. Collaborate with other Medical Heads across Oncology and Biopharma/Cell Gene and with senior leadership of Clinical Operations, Quantitative Sciences, Regulatory and Pharmacovigilance/Medical Safety in the development and maintenance of medical science specific global standards, processes, SOPs, training and quality control, to the highest level of compliance with ICH, GCP and Astellas policies.. Play a strategic lead role, in collaboration with Research, Regulatory Affairs and Early Development and Translational Sciences, to ensure optimal strategic and quality input and delivery in planning of clinical development strategies, execution of clinical trials and in the preparation and submission of relevant regulatory dossiers, documents, presentations, health authority responses and specialty publications.. Significant experience in drug development in pharma or pharma and/ or as a clinical investigator in academia, particularly in the Oncology Solid Tumor development space.
Under the direction of the manager, enters information, i.e., encounter form charges, cash payments-both patient and insurance payments- as well as insurance rejections to the Accounts Receivable system.. Inputs cash payments, i.e., responsible party commercial insurance, co-payments, Medicaid, Medicare, Blue Shield, Out of State Blue Shield, Medex, and lock box payments.. Performs on line cashiering functions including automated cash application and as well as manual cash receipts.. Maintains back up copier of encounter forms by doctor and date.. Strong typing skills and previous experience with medical billing for third party payment desired Network Information Exchange Access Level: 0
Reporting directly to the President of AWP HealthCare, this role is directly responsible for the daily clinical operations of the entire pharmacy department and the management of personnel including Staff Pharmacists, Inventory Specialists, Pharmacy Technicians, and Courier Services.. This role acts as the designated Manager of Record/ Pharmacist in Charge for all states in which AWP Pharmacy- Billerica holds a valid, active pharmacy license.. · Manage the daily operations of AWP’s Pharmacy Production Department, including oversight of pharmacy supervisors, staff pharmacists, inventory specialists, pharmacy technicians, pharmacy technician trainees, and pharmacy interns. · Ensures staffing levels are appropriate to meet departmental service level agreements and maintain regulatory required pharmacist: technician ratio at all times. Advanced Wellness Pharmacy (AWP) is proud to be a leading provider of multi-dose compliance packaging and medication management servicing a high-risk patient population.
Zenas BioPharma is a global biopharmaceutical company committed to becoming a leader in the development and commercialization of immune-based therapies for patients worldwide.. 7+ years of medical writing experience in pharma, biopharma, or CRO.. Track record of contributing to successful regulatory filings (IND/CTAs, NDA/BLA/MAA).. Knowledge of biologics, clinical research, study design, biostatistics, and medical terminology.. Proficiency in Microsoft Office, with experience in Veeva Vault and AI writing tools a plus.
Obtain necessary pre and post treatment vital signs and weight and perform vascular access evaluation pre- treatment. Evaluate patients’ vascular access during treatment including arterial and venous monitoring pressures, provide appropriate intervention as needed, document and report any unusual findings to the registered nurse or supervisor.. Ensure collection of lab specimens by appropriate lab courier.. Assists in assuring patient understanding or home dialysis products, benefits of home and how home dialysis can work for them.. Assist in assuring patient understanding of treatment options including demonstration of the peritoneal dialysis set-up.
Duties Description The incumbent will provide nursing services and care to patients, including medication administration, specimen collection (blood and urine), assessment of patient needs, treatment planning, nurse teaching, building security, crisis intervention, and related documentation.. Nurses provide 24-hour, across-shift communication and care consistent with licensing standards and NYS regulations.. Minimum Qualifications Registered Nurse 1 Psychiatric: possession of a license and current registration to practice nursing in New York State.. Candidate must be eligible and maintain eligibility for full and unconditional participation in the Medicaid and Medicare program.. Failure to maintain licensure, certification and Medicaid/Medicare eligibility will result in the termination of employment.
Senior Principal Scientist, Precision Medicine, Immunology. Precision Medicine is an integral part of our Immunology Therapeutic Area. To support our growing Immunology pipeline across Gastroenterology, Rheumatology and Dermatology we are seeking an experienced experimental medicine leader in our newly created Precision Medicine and Diagnostics function.. Work closely with a cross-functional group of experts, including clinical directors, clinical trial operations, and biomarker operations teams as they key liaison to enable implementation of precision medicine strategy in clinical trials. Collaborate with discovery colleagues for programs in early stage to influence biomarker assessments and readouts to drive forward and reverse translation tied to Precision Medicine goals. Bioinformatics, Bioinformatics, Biomarker Research, Clinical Development, Clinical Immunology, Clinical Medicine, Clinical Research, Clinical Testing, Clinical Trial Management, Cross-Cultural Awareness, Cross-Functional Teamwork, Dermatology, Drug Development, Ethical Compliance, Ethical Standards, Immunoassays, Immunotherapy, Management Process, Medical Research, Mentorship, Parasitology, Patient Care, Professional Networking, Protocol Development, Regulatory Compliance {+ 4 more}
PhD in biology, biochemistry, or a related discipline and 6+ years of related industry experience, with a demonstrated focus on lipidomics/metabolomics.. Extensive knowledge and experience with lipidomics and metabolomics approaches and technologies, with key applications in biomedical and translational research, including neuroscience, cardiovascular, renal, diseases of aging, and oncology research. Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Decision Making, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy- Leadership, Influence, Laboratory, Lifesciences, Machine Learning (Ml), Medical Research, Mentorship {+ 11 more}