- Novo Nordisk Inc. (Plainsboro, NJ)
- …ready to realize your potential? The Position The Senior Analyst will be the Master Data Management (MDM) primary Subject Matter Expert (SME) for Market Access and ... Manager for Data Stewards of Patient, Customer and Product masters . Role will also be responsible for day-to-day support...how to use the MDM tool to maintain NNI master data and business rules. This position will also… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based ... Role Overview We are actively seeking a proficient SAP Master Data Sr. Specialist with a specific focus on...IT team and collaborate in the design-implementation of Legend's Master Data Management program. We are looking for a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Guild Lead has a team of agile coaches and agile scrum masters . Essential Functions Agile Transformation Leadership: Lead Novo Nordisk's agile transformation efforts ... and Training: Provide guidance, mentorship, and coaching to Agile teams, Scrum Masters , CS&M leadership, and other stakeholders to enhance their understanding and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …preferably in a scientific discipline; requiredan advanced degree (eg, Masters , Pharm.D., Ph.D.) preferred Experience Qualifications10 or More Years pharmaceutical ... Degree preferably in a scientific discipline requiredadvanced degree (eg, Masters , Pharm.D. or Ph.D.) preferred Experience Qualifications7 or More Years… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …including limited international travel. Qualifications Education Level: Bachelor's degree required; Masters Preferred Experience Level: 5+ years of experience in a ... of digital solutions; four (+4) years of relevant experience with a Masters may also be considered; relevant experience in Business Development, Investment, Venture… more
- Aequor (Thousand Oaks, CA)
- …(Occasional meetings early mornings or later in the afternoon) Ideal Candidate: Bachelors or Masters . would be wonderful if they can have a CSCP cert. Experienced in ... conjunction with site as needed Creates and maintains source master data in SAP and Rapid Response Review network-wide... data in SAP and Rapid Response Review network-wide master data and address issues with appropriate data owners… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …maintain all required study programming documentation required for Trial Master File (TMF)- Maintain institutional knowledge across oncology compounds and ... reasonable accommodation.Education /Qualifications (from an accredited college or university)- Master 's Degree Biostatistics or similar degree required- PhD Biostatistics… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …university)Bachelor's Degree preferably in a scientific discipline requiredAdvanced degree (eg, Masters , Pharm.D., Ph.D., MD, Advanced degree (eg, Masters , ... Pharm.D., Ph.D., MD, JD) preferredExperience Qualifications7 or More Years relevant pharmaceutical experience including experience within Regulatory AffairsUnderstanding of scientific content and complexities and good knowledge of diagnostic development,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …accommodation. Education /Qualifications (from an accredited college or university)- Master 's Degree in statistics or biostatistics required- PhD in statistics ... 10+ Years of relevant experience in the pharmaceutical industry with a masters degree required- 7+ Years of relevant experience in the pharmaceutical industry… more
- Aequor (San Diego, CA)
- …with at least 2-4 years work experience in the Pharma industry. Masters degree acceptable. PhD candidates will not be considered. Demonstrate proficiency with ... sterile cell culture, cell-based assays (CTG, apoptosis) and molecular biology techniques (Protein, DNA and RNA isolations, Western blot, qRT-PCR, Flow Cytometry) Experience with high-throughput drug screening is a plus Possess some trouble shooting and… more
- Merck & Co. (Rahway, NJ)
- …portfolio outside of their assigned programs. Position Qualifications: Education Minimum Requirement: - Masters with a minimum of 15 years or Ph.D. with a minimum ... of 12 years of industry experience and a Degree in Chemical/ Biomedical Engineering, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemistry, Biochemistry or related field.- Required Experience and Skills: -The candidate should have a… more
- Merck & Co. (Rahway, NJ)
- …expectations and processes for data product owners, data analysts and scrum masters .Leverage data domain knowledge to shape the vision, strategy, and roadmap of ... domain level analytics ready datasets.experience in large scale multi country program rollout with cross divisional and market stakeholdersStrategic thinking, risk management, and roadmap planning for data product evolutionEnsure implementation of Agile… more
- Aequor (Swiftwater, MN)
- …include supporting Business and IS LIMS Administrators in report design and build, updating master data for new and existing products, updating master data for ... improvement, and to support laboratory informatics needs. Support the creation of New Master Data for new LabWare System build for EM ONE LIMS Global System.… more
- Aequor (Seattle, WA)
- …or relevant scientific discipline with at least 5 years of relevant experience / Masters ' degree with a minimum of 2-6 years of relevant experience Highly motivated ... self-starter that works well both in teams as well as independently Strong project management, business process management, and optimization skills Familiarity with end-to-end CMC drug development with an understanding of critical milestones and typical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …accredited institution in a science or in a technical field preferred- Master 's Degree preferred Experience Qualifications- 10 or More Years proven experience within ... or CROs supporting statistical analysis of clinical trials programming with Masters degree preferred- Previous experience supporting SAS macro and/or system utility… more
- Aequor (West Greenwich, RI)
- Not looking for overqualified candidates with a masters or PHD. Ideally looking for candidates with at least 2 years of an associate degree combined with 2 years of ... General lab experience/lab background, GDP/GMP experience and or a bachelor's degree also paired with General lab experience/lab background, GDP/GMP experience. Looking for local candidates local to the New England area, exclusively as the EW will be coming… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …guidance for the validation program, Policies and SOPs and other master documentsSupport Engineering and Manufacturing in the development of critical process ... and timeliness of their deliverablesEducation and Experience Requirements: Bachelors, Masters , or Ph.D. in Biochemistry, Biology, or related science… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an accredited college or university)Bachelor's Degree required.Advanced degree (eg, Masters , PharmD., Ph.D., MD, JD) preferred. Experience Qualifications:10 or More ... Years in the pharmaceutical industry required.7 or More Years in regulatory affairsExperience in providing regulatory strategic input into the drug development process with thorough knowledge of the IND and NDA/BLA processes.Ability to interpret and understand… more
- Merck & Co. (North Wales, PA)
- …stakeholdersPartner with squad members including but not limited to scrum masters , technical lead(s) and development team to manage high-quality product delivery ... leveraging Agile SDLC methodology.Work closely with stakeholders to ensure a healthy backlog of well-formed epics, features and user stories are maintained, which align with the overall roadmap and serve as requirements for the delivery squad.Follow and apply… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in medicine, life sciences, health or related field requiredAdvanced degree Eg, Masters , Pharm.D., Ph.D., MD, JD preferred Experience Qualifications7 or More Years ... Experience in pharma Regulatory Affairs, with at least 3 years developing regulatory strategies incl. successful delivery of regulatory projects submissions, and a working knowledge of global regulations and guidelines regarding drug development (incl. CMC),… more
