- Merck & Co. (North Wales, PA)
- … trial agreements, confidentiality agreements, and other type of agreements related to clinical research.As a GSA Specialist you will work closely with ... as liaison to Office of General Counsel, Privacy, Compliance and Clinical Teams, as appropriate,to resolve contractual/legal issues with sites, investigators, and… more
- Merck & Co. (Rahway, NJ)
- …of the study protocol as well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. Support the ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...or other applicable legally protected characteristics. - For more information about personal rights under the US Equal Opportunity… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our Company's ... Research Laboratories portfolio of clinical trials. GCS is accountable for the planning, sourcing,...or other applicable legally protected characteristics. - For more information about personal rights under the US Equal Opportunity… more
- Merck & Co. (Memphis, TN)
- Job DescriptionOur Sales team support our customers by providing clinical information about products, educational information , clinical training programs ... environment and are driven to succeed. The Oncology Sales Specialist (OSS) is a key member of our customer...and communicating our vision to the larger Oncology community.Territory Information : This position covers all of Arkansas, parts of… more
- Novo Nordisk Inc. (Boston, MA)
- …as a frontrunner in the cardiometabolic care market. The Ecosystem Portfolio Specialist is responsible for achieving sales targets by effectively promoting Novo ... adherence to approved guidelines. Relationships Externally, the Ecosystem Portfolio Specialist maintains relationships with physicians, pharmacists, nurses, and other… more
- Novo Nordisk Inc. (Philadelphia, PA)
- …Generate advocacy for Novo Nordisk products and services by sharing approved clinical and scientific information and insights Analyze and leverage understanding ... assess, create and maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes local tactical plans… more
- Novo Nordisk Inc. (Denver, CO)
- …gain access and drive business impact by collaborating around the clinical management of patients and offering NNI-approved solutions Demonstrates professionalism ... and competitor products Demonstrates thorough knowledge of all promoted NNI approved clinical studies and the skill to engage customers (prescribers, support staff,… more
- Merck & Co. (Rahway, NJ)
- …or related fields.3+ years in Project and/or Program Management supporting Information Technology, or Pharmaceutical Research or Clinical Trial Operations ... or Product Owner certificationPrior experience in the pharmaceutical industry or Clinical Trial Operations or Information Technology.Basic understanding of the… more
- Novo Nordisk Inc. (Worcester, MA)
- …Generate advocacy for Novo Nordisk products and services by sharing approved clinical and scientific information and insights Interface with key associations ... The EDCS must achieve sales goals by utilizing a patient-centric and clinical approach to engaging their customers and promoting Novo Nordisk's portfolio of… more
- Merck & Co. (Rahway, NJ)
- …Research Infrastructure Product Line (RIPL) engineering team is seeking a Senior Specialist - Research Automation OT Infrastructure. This position will be a member ... product (Laboratory and Plant) within RIPL. -As Sr. OT Infrastructure Specialist , you will lead the definition and implementation of high-level requirements,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... living. Are you ready to make a difference? The Position The Labeling Specialist supports the development of labeling activities for all regulatory submissions. This… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Maintenance Specialist I (2nd and 3rd shift) as part of the Facilities & Engineering ... be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift. This… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Senior CQV Specialist as part of the Commissioning and Qualification team based in Raritan, NJ. ... for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Quality Project Management Specialist as part of the Quality team based in Raritan, NJ. Role ... improvement projects within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …engagements and develops and executes strategies to identify and fulfil complex information needs company-wide using advanced clinical informatics tools and ... techniques. This role requires a deep understanding of both clinical workflows and information technology. Relationships This...of Clinical Informatics and functions as a clinical informatics specialist in the Clinical… more
- Merck & Co. (North Wales, PA)
- …to support holistic portfolio management and increased integration of CMC and Clinical strategies . - Position Description/Summary: - The CIPM Associate Director, ... optimized for the portfolio. Build and maintain project schedules and critical project information , us ing these tools to integrate activities across key functional… more
- Merck & Co. (Rahway, NJ)
- …includes integrating strategic and tactical input from diverse disciplines (eg, clinical , regulatory, market access, manufacturing, CMC, commercial, and other areas) ... the project. - Building and maintaining project schedules and critical project information in enterprise project management systems and databases. Using these tools… more
- ECLARO (Warren, NJ)
- Specialist , QA Engineering Job Number: 25-03449 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Specialist , QA ... manufacturing facility. This team supports the Cell Therapy Development early clinical drug product manufacturing facility, which supplies autologous and allogeneic… more
- Medical Mutual of Ohio (OH)
- …full remote Serves as business unit project lead in professional writing for Clinical Quality and Health Services (CQHS) and Pharmacy Department responses for the ... Pharmacy programs. Evaluates and updates answers quarterly and annually with clinical staff to ensure accuracy and consistency in messaging. **Responsibilities** +… more
- Tomah Health (Tomah, WI)
- …to mentor and assist staff in professional growth. JOB REQUIREMENTS * The Information Systems Clinical Application Specialist is frequently required to ... to sit, climb or balance, stoop, kneel and crouch. * The Information Systems Clinical Application Specialist must occasionally lift and/or move up to… more
