- Merck & Co. (North Wales, PA)
- …Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible for ... independent compliance support of Medical Devices including the device constituent part of Combination Products. This position will interact with cross functional teams working with all levels of employees. Activities will include developing, documenting, and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Value Access & Pricing will both develop and ... execute the market access and pricing strategies for the assigned asset. This person will own the pricing and access strategy for the assigned oncology asset(s). This person will report to the Sr Director, Global Oncology Value Pricing & Access, and will be… more
- Aequor (South San Francisco, CA)
- …Maintain virus inventory and registry using informatics platform such as the Benchling system. Assist with viral vector technology development and application for in ... vitro or in vivo genome engineering by CRISRP/Cas9 system. Work independently within a dynamic, highly collaborative research environment. Skills Proficient in mammalian cell culture and general molecular biology techniques such as transient plasmid… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the Quantitative ... Clinical Pharmacology (QCP) group to develop and apply QSP models to aid in drug discovery/development decisions, which include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she… more
- Aequor (Thousand Oaks, CA)
- …more of a preference. We can train candidates on our QMTS roles. Associate Supply Chain Description: Candidates will, under limited supervision and in compliance ... with clinical regulatory requirements, partner with key stakeholders to manage shipments of clinical drug product to clinical sites, globally. Key Responsibilities and Activities General: - Provide distribution support to Global Supply Planners and Logistics… more
- Aequor (South San Francisco, CA)
- Job Title : Research Associate I Location : South San Francisco, CA Duration : 1 year Job Description We are seeking a highly motivated individual Scientist 1/3 to ... join the Department of Preclinical and Translational Pharmacokinetics and Pharmacodynamics (PTPK). (S)He will be part of the PK technology/operations group and will be supporting the larger PTPK department in their execution of PK studies of molecule… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical ... Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. Job Summary The Associate Director, Omnichannel Marketing Platform Technologist serves as the omnichannel business partner ... for Eisai marketing and brand teams. As the leader of the digital channels including email and web channels, he/she/they works with business stakeholders to design omnichannel solutions to meet the strategic marketing needs of the business.In this role,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …that fall under the responsibility of the R&D Procurement group. The Associate coordinates with R&D Procurement team members, Purchasing, Legal, Finance, vendors and ... other functional groups as needed. This role performs contract execution, new vendor set-up and maintenance, simple negotiations, prepares for audits and inspections, troubleshoots payment delays, and other duties as needed.Responsibilities- Contract… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug/vaccine clinical ... development projects.- Accountability predominantly includes the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual… more
