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Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care. Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources. Manages clinical denials, educating referring providers on clinic and payor requirements. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse’s specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years). As part of our commitment to our patients and employees’ wellness, Parkland Health is a tobacco and smoke-free campus.
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care.. - Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources.. Manages clinical denials, educating referring providers on clinic and payor requirements.. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse's specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years).. As part of our commitment to our patients and employees' wellness, Parkland Health is a tobacco and smoke-free campus.
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.
The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.. Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications. Oversee medical and scientific review of promotional materials for GRC and MRC. Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials. Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred.
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.. Referral services for child, elder and pet care, home and auto repair, event planning and more. Healthcare experience should be recent and within a clinical setting such as Hospital, Ambulatory Surgery Center, etc.. Other specialized programs include our Sleep Center at Fairview Park, the Same Day Surgery Center, the Heart Center at Fairview Park, the Women's Imaging Center and much more.. HCA Healthcare Co-Founder
The Patient Care Technician position on G18- Stem Cell Transplantation & Cellular Therapy unit at MD Anderson Cancer Center provides patient care services as assigned by a registered nurse, and directly impacts patient comfort and outcome of care. Ideal candidate must have a high school diploma and either one year of recent experience in an acute care setting as a Nursing Assistant or a CNA certification. The Inpatient Stem Cell Transplant & Cellular Therapy unit is a 48 bed unit and is one of our designated immunotherapy floors, administering research protocols involving immunotherapy and CARTOX therapy to patients, including Phase 1 clinical trials. Teachers Retirement System defined-benefit pension plan and two voluntary retirement plans.. Relocation Assistance Available?
Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.. Training will require working the AM shift for 2-3 weeks.. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.. Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
+ 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)
Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.. Training will require working the AM shift for 2-3 weeks.. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.. Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
The Frederick National Laboratory is operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.. Within Leidos Biomedical Research Inc. (operator of the Frederick National Laboratory for Cancer Research), the Clinical Research Directorate (CRD) provides clinical supervision of programs at the clinical end of the research spectrum.. CRD also provides operational support for clinical research and supports clinical trials management, regulation, pharmacovigilance, and protocol development/protocol navigations.. Provides inpatient and outpatient consultative Infectious Disease care for Hematopoietic Stem Cell Transplant (HSCT) Patients. Board certification in Internal Medicine and Allergy and Immunology or Infectious Diseases (other Internal Medicine specialty training will be considered)
Verovian Healthcare Recruitment Agency is seeking skilled and motivated Nursing Informatics Specialist (RN) for a full-time role in Tucson, Arizona. Collaborate with clinical and IT teams to implement and maintain healthcare informatics systems. Bachelor's Degree in Nursing (BSN) required, advanced degrees in Nursing Informatics or a related field preferred. Strong understanding of clinical workflows and healthcare informatics systems. With Verovian Nursing Recruitment Agency, you will gain exclusive access to premier healthcare opportunities that align with your career goals.
-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
You will supervise nursing care provided by registered nurses, licensed vocational/practical nurses and STNA/CNAs.. - Director of Nursing, management or supervisor experience in long-term care, restorative or geriatric nursing.. About Ciena Healthcare. Ciena Healthcare is Michigan’s largest provider of skilled nursing and rehabilitation care services.. If you have a passion for improving the lives of those around you and working with others who feel the same way, Ciena is the place for you!
Join to apply for the Consultant, Healthcare & Life Sciences role at Simon-Kucher. Our Healthcare & Life Science Division works across the highly innovative, complex healthcare sector, including pharmaceuticals & biotech, medical technology, diagnostics, digital health & healthcare IT, healthcare B2B, providers, consumer health, and animal health.. Has obtained or is currently enrolled in an undergraduate or graduate degree program at an accredited university/college pursuing a degree in biology, chemistry, biochemistry, or pharmacology, or a related sciences or business field. Strategy Associate Consultant - Healthcare Consultant, Life Sciences Process & Procedures (Pharma/Biotech) Boston, MA $85,000.00-$150,000.00 2 weeks ago. Practice Transformation Coach, TEAM UP Scaling & Sustainability Center Senior Consultant – Healthcare & Life Sciences, Commercial Strategy Boston, MA $250,000.00-$265,000.00 2 weeks ago
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
Research and decipher regulatory sources such as legislative rules, stateregisters, waiver programs and bulletins regarding payment rules for State Medicaid programs as well as deciphering contractual language regarding commercial payment arrangements.. Bachelor's degree or equivalent experience in healthcare administration, business administration, or a related field. Five+ years of experience in Medicaid billing, reimbursement, claim payment or cost reporting.. Experience with Medicare/Medicare Advantage or commercial billing and reimbursement a plus. Proficient Microsoft Office skills (i.e., functions, macros, pivot tables, data validation, business requirement writing, etc.)
As the Associate Director, Clinical Quality Assurance (CQA), you are a key member of the Clinical Quality team maintaining representing Clinical QA in cross functional setting, and advising Cytokinetics Clinical Operations, Biometry and Drug Safety and Pharmacovigilance teams on Clinical Quality matters.. Provide expert CQA advice and strategic mentorship to stakeholders (e.g. Clinical Operations, Data Management, Pharmacovigilance) to support regulatory inspections.. Current and strong working knowledge, interpretation/implementation United States Code of Federal Regulations and European regulations and guidance, including ICH-GCP Guidance requirements governing clinical research conduct and pharmacovigilance operations. Experience with electronic Quality Management Systems and Trial Master File.. Experience in hosting or supporting clinical trial or Drug Safety-related regulatory inspections a plus.
Reporting to the Chief Medical Officer, the Pharmacovigilance Scientist at Cellectis will manage all activities related to the performance of drug safety at Cellectis.. drug safety is pro-actively integrated into drug development activities. Manage interface with drug safety meetings (PV team, DSMB/DMC and SAC meetings). Educate the organization on critical developments and regulatory guidance related to drug safety (FDA, EMA, MHRA, PMDA and others, where necessary). Minimum of 7-10 years of relevant experience in pharmacovigilance, drug safety, regulatory affairs or clinical trials
Responsibilities Clinical Program Leadership: Design, implement, and medically monitor clinical trials (Phase 1-3) for oncology assets.. Cross-functional Collaboration: Work closely with research, preclinical development, regulatory affairs, biostatistics, data management, clinical operations, and commercial teams to ensure seamless program execution.. Minimum of 10+ years of clinical drug development experience in the biotechnology or pharmaceutical industry, with a focus on oncology biologics.. Demonstrated success in leading and managing clinical trials from early to late-stage development.. Strong understanding of clinical trial design, biostatistics, medical monitoring, and regulatory requirements (FDA, EMA, ICH guidelines).
The Clinical and Translational Institute at West Virginia University is currently accepting applications for a (Hybrid) Clinical Research Specialist located in Southern West Virginia.. Participates in the development, coordination, and implementation of research and administrative strategies essential to the successful management of Phase II/III/IV clinical trials research conducted by investigators within the National Institutes of Health (NIH) CARE for HealthTM initiative, which is a pilot to test the feasibility of a network to embed clinical research in primary care settings.. Human subjects protection and related issues - knowledge of professional principles (GCP and IRB guidelines), legal and/or reporting requirements affecting grants and contracts, and adheres to industry and government standards.. Within two (2) years of employment, incumbent must obtain certification as a Research Coordinator through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA).. From the groundbreaking R1 research at our flagship campus in Morgantown to the career-oriented programs at WVU Potomac State in Keyser, and the technology-intensive programs at WVU Tech in Beckley, the contributions of WVU employees resonate across the state, touching lives and shaping futures.