Clinical Account Manager- Northeast Region Route 92 Medical IncClinical Account Manager- Northeast RegionNewark, NJPlans, directs and coordinates activities to drive support of product use within a designated geography or list of accounts • Promotes safe and effective use of Route 92 technology to include case coverage and product demonstration • Coordinates training activities for accounts within the designated geography to include onsite customer education and in-servicing • Collaborates with Territory Managers within each territory to drive Route 92 product adoption and advocacy • Has responsibility for service activities in support of sales process • Collaborates internally with the team to continually strengthen the culture and enhance customer relationships • Monitors competition by gathering current marketplace information on pricing, existing and new products & sales strategies • Recommends changes in products, services, and policy by evaluating results and competitive developments • Maintains professional and technical knowledge by on-the-job training, attending educational workshops, reviewing professional publications, establishing personal networks and by participating in professional societies. • Candidate must be located in the North East region or relocating to the region prior to hire • Flexible, able to pivot in fast-paced environment • Strong communicator with ability to digest and communicate clinical information and report out to colleagues • Demonstrated understanding of clinical environment, products, and players in the neurovascular market • Public presentation experience • Strategic thinker who takes initiative, self-starter, and builds own value within role • Active listener with customer focus • 50%+ ability to travel.
Senior Analyst Clinical Data Systems AbbVie IncSenior Analyst Clinical Data SystemsFlorham Park, NJApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
System Associate Medical Director, Heart Failure Program - Atlantic Health Atlantic Health System IncSystem Associate Medical Director, Heart Failure Program - Atlantic HealthMorristown, NJ$500,000–$750,000 / yearWe offer excellent clinical, academic, and clinical research opportunities as well as the opportunity to help establish the vision for a heart failure program that oversees care at each of Atlantic Health's hospitals and coordinates outpatient care through Atlantic Medical Group's large multispecialty practice. Atlantic Health Morristown's Department of Cardiovascular Medicine, housed within the 200-bed Gagnon Cardiovascular Institute, is a leader in cardiovascular care in New Jersey and offers a full spectrum of cardiovascular services.
Research Coordinator NYU Langone HealthResearch CoordinatorNew York, NY$66,299.99–$68,250Full timeHuman Subjects' Research - As applicable, oversee the submission of necessary documents required by the NYU Institutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination). Responsible for providing moderate to advanced range of coordination of Research studies conducted at the Medical Center, assists with the recruitment, enrollment, grant submissions, research data collection and study coordination activities.
NewResearch Coordinator, Obstetrics and Gynecology (OBGYN) NYU Langone HealthResearch Coordinator, Obstetrics and Gynecology (OBGYN)New York, NY$66,300–$69,300Full timeFertility and Biospecimen Research Support: Supports biospecimen-related research activities, including specimen inventory and tracking, consent logging, continuing review reports, study audit support, participant follow-up regarding research consents, and coordination related to research sample storage, tracking, and relocation. Contribute to the Departments coordinated research support model by supporting multiple assigned studies, balancing competing priorities, and adjusting work as needed based on study timelines, participant needs, operational demands, and departmental research priorities.
Clinical Supply Chain Associate (Cobble Hill-Brooklyn) (M-F 12p-8p) NYU Langone HealthClinical Supply Chain Associate (Cobble Hill-Brooklyn) (M-F 12p-8p)Brooklyn, NY$50,204.70–$51,000Full timeCreate requisitions and scan par location supplies for use operating/procedural rooms: Manual requisitions, Rush Orders, Special Requests, Consignment Orders, Bill Only POs, No Charge POs (trials/consignments). has ranked NYU Langone the No. 1 comprehensive academic medical center in the country for three years in a row, and U.S. News & World Report recently placed nine of its clinical specialties among the top five in the nation.
Director, Clinical Science Lantheus Holdings IncDirector, Clinical ScienceNY$191,000–$286,000 / yearContribute to authoring and lead design/reviews of key product and study-related documents and deliverables, including but not limited to Clinical Protocols and amendments, Investigator Brochures, Study Manuals, Case Report Forms, Informed Consent Forms, Clinical Study Reports, Annual Reports, regulatory submissions, abstracts and publications. Interacts with internal and external stakeholders (Key Opinion Leaders, Medical Director, vendors, committees) in support of clinical trial objectives and deliverables, including investigator-sponsored trials.
Clinical Strategy Lead for Digital Endpoints SanofiClinical Strategy Lead for Digital EndpointsMorristown, NJ$178,500–$257,833.33 / yearRelevant experience includes Life sciences, pharmaceuticals, clinical data analysis, clinical trial design, medical imaging, novel endpoint design, clinical outcomes assessments, academia, or related field and/or digital health technologies contributing to a solid grasp of the intersection of clinical development and digital health technologies. The Clinical Innovation team includes our digital biomarker strategy and operations team which focuses on establishing and executing digital biomarker programs that generate health-related data through digital health technologies (DHTs), provide valuable insights into patients' conditions, and aid in improving the clinical trial experience.
Sr. Medical Director, Clinical Development Kyverna Therapeutics IncSr. Medical Director, Clinical DevelopmentNYRemote$330,000–$370,000 / yearServe as the physician lead for CAR T-cell therapy clinical trials in autoimmune disease indications, in partnership with internal and external cross-functional teams. This salary range is an estimate of what we reasonably expect to pay for this posted position, and the actual salary may vary based on various factors, including without limitation individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.
Director Clinical Development, Solid Tumors, GI BeOne Medicines AGDirector Clinical Development, Solid Tumors, GINY$249,800–$309,800 / yearThe Director, Clinical Development will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical development role.
Director, Clinical Data Management, Global Data Management and Standards Merck & Co IncDirector, Clinical Data Management, Global Data Management and StandardsRahway, NJ$173,200–$272,600 / yearEnterprise Leadership Skills: Innovation | Challenge current thinking-Explore alternative ways to view and solve problems and achieve results; leverage innovation tools, creative processes and different cross-functional experts to generate ideas; combine ideas in unique ways; make times to incubate ideas; thoughtfully evaluate alternatives and then select the best ideas for experimentation. Experience managing clinical data management processes including eCRF (electronic Case Report Form) design, clinical database development and validation, user acceptance testing, external data management, data extraction, data transformation to SDTM, and analysis & reporting.
Director Clinical Development, Solid Tumors BeOne Medicines LtdDirector Clinical Development, Solid TumorsNY$249,800–$309,800 / yearThe Director, Clinical Development will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical development role.
Principal Clinical Content- Physician - UpToDate®, Physician Editor, Adult Neurology Wolters Kluwer N.V.Principal Clinical Content- Physician - UpToDate®, Physician Editor, Adult NeurologyNew York City, NY$173,500–$310,000 / yearUpToDate editors work closely with outside authors, section editors, editors-in-chief, and peer reviewers to ensure the material is accurate and free of bias. In the remaining 10 to 20% time, Physician Editors should continue patient care activities, using their clinical experience to help ensure the content of the program is maximally useful at the point of care.
Principal Business Analyst - Research Program Management Regeneron Pharmaceuticals IncPrincipal Business Analyst - Research Program ManagementTarrytown, NY$114,800–$187,400 / yearBuild our future together: The Principal Business Analyst Research Program Management (RPM), will work collaboratively with Research Program Managers, Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific drug discovery and data processes and translate these into requirements for the development of data and technology solutions that support Regeneron's scientific mission. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data and process modeling frameworks) in order to perform business analysis, elicit and document requirements, map data flows, and drive data quality improvements in a research-focused environment.
NewSenior Clinical Trials Budget Analyst - Remote VitaliefSenior Clinical Trials Budget Analyst - RemoteNew Brunswick, NJRemote$75,000–$125,000 / yearBy combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients. About Vitalief Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing consulting, staffing, and technology-enabled services to academic medical centers, health systems, sponsors, CROs, and site networks.
Executive Medical Director, Neurology, Clinical Development Karwell TechnologiesExecutive Medical Director, Neurology, Clinical DevelopmentBridgewater, NJThis individual will be the primary point person for medical monitoring and oversight of assigned clinical programs, including monitoring of clinical studies, review and interpretation of clinical trial data, authoring clinical study and regulatory communications and documents, and monitoring of competitor activities and data. Provide medical/clinical expertise to internal (Marketing, Sales, Manufacturing, Market Access, Patient Services, Regulatory Affairs, R&D, and Legal) and external (healthcare professionals, Data Safety Monitoring Boards, patients, advocacy groups, etc.) customers.
Forward Deployed Product Manager - AI Iterative Scopes IncForward Deployed Product Manager - AINew York, NY$170,000–$250,000 / yearWe built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors'' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Associate Director, Health Authorities ImmunityBio IncAssociate Director, Health AuthoritiesSummit, NJCreate and maintain project plans for health authorities operations • Participate in cross-functional teams and provide support to others in the preparation, analysis, and documentation of studies • Lead external stakeholder engagement throughout the submission lifecycle, coordinating with CROs, external regulatory consultants, and subject matter experts / key opinion leaders to gather data, craft high‑quality RFI responses, and foster constructive agency relationships • Prepare and assign responses to Health Authority comments and questions pertaining to clinical issues. Education & Experience • Bachelors Degree in life sciences or technical discipline with 10+ years of relevant progressive experience required; or • Masters Degree in life sciences or technical discipline with 8+ years of relevant progressive experience required; or • Doctorate degree in life sciences or technical discipline with 6+ years of relevant progressive experience required.
Research & Development Specialist ACM Global Central Laboratory LtdResearch & Development SpecialistNY$70,000–$80,000 / yearEnsures all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP) etc. For disease specific care programs refer to the program specific requirements of the department for further specifications on experience and educational expectations, including continuing education requirements.
NewNurse Practitioner - Kidney Transplantation/ Xenotransplantation Research - Manhattan - 10hr days NYU Langone Medical CenterNurse Practitioner - Kidney Transplantation/ Xenotransplantation Research - Manhattan - 10hr daysNew York, NY$151,530.94–$182,030.94 / yearFormulates a plan of care, along with the attending physician, consulting physicians, the research team, patient, family, and other members of the interdisciplinary team for both preoperative and postoperative transplant patients, based on expected goals of care and length of stay, care that maximizes individual patient/family preference and enhances quality, access, and cost-effective outcomes. Performs complete health history, physical examination, and psychosocial assessment of pre- and post-operative transplant patients, primarily xenotransplant patients, in the outpatient clinic.