- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …support the leader in the development and implementation of the Compliance Monitoring Program, specifically Federal healthcare laws, FDA promotional guidelines, and ... laws, guidelines, and regulations. This individual will partner with members of the Compliance team on critical projects and provide support; will be responsible for… 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… more
- Merck & Co. (Rahway, NJ)
- …Code of Conduct and the Ethics Ambassador Program, developing ethics and compliance training workshops and communications, and managing other key initiatives in ... candidate's ability to work effectively with colleagues within the Ethics and Compliance Office (ECO) and across divisions, functions, and regions. This position… more
- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Associate Director - Process/Facility Engineering position will report to the Director, ... infrastructure.- Responsibilities include the following:The process/facility engineer role at the Associate Director level will serve as a technical mentor and… more
- Aequor (Thousand Oaks, CA)
- …analysis for effective decision making in NA-TO Hub Manage and oversee Compliance related activities Develop strategic and tactical processes that increase the ... or Business experience preferably in the biotechnology or pharmaceutical industry OR Associate 's degree and 6 years of Life Science or Business experience preferably… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... at our company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as applicable to the… more
- 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...audits of data, policies, procedures, and systems to ensure compliance with Medical Device (21CFR 820s) and Combination Product… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Omnichannel Marketing and Media position reports to the Senior Director, Omnichannel ... Marketing (HCP and Patient). The associate director will also partner closely with key internal...across target audiences as well as ensure regulatory/legal and compliance requirements are met.This role requires strong marketing and… more
- Merck & Co. (Boston, MA)
- Job DescriptionWe are seeking an experienced and innovative Associate Principal Scientist with a strong background in In Vitro Pharmacology to join the External ... in partner site visits to evaluate processes, capabilities, safety procedures and compliance standards as well as build workflows to compliment internal company… more
- Merck & Co. (Rahway, NJ)
- …to lead and support facility operations, process development activities, compliance investigations/change management, authoring of GMP documentation, and lead other ... initiatives as appropriate. Collaborate closely with development engineers & chemists, compliance representatives, and other team members to ensure the quality 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 ... strategies and pricing policies; in collaboration with key regions/markets Ensure compliance with legal requirements- Collaborate and provides input to Clinical on… more
- Eisai, Inc (NJ)
- …this is your profile, we want to hear from you. Job Summary The Associate Director, Clinical Outsourcing, will oversee and lead and support activities related to the ... and functional service providers for Eisai's R&D functions. This role will ensure compliance with key processes and manage the outsourcing team. The ideal individual… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of research and strategic partnership contracting agreements. In collaboration with the Associate Director, the Associate Manager will support CMR's partnership ... internal and external stakeholders Relationships This position reports to an Associate Director overseeing the contract management function of the CMR organization.… 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
- Merck & Co. (North Wales, PA)
- …future contracts.Working with sales teams and customers to ensure appropriate compliance with the terms and conditions of our contracts.Collaborating with ... manufacturing and distribution teams to ensure internal contract compliance .Collaborating cross functionally to design tactics to support account management and… more
- Merck & Co. (North Wales, PA)
- …Account Management , Learning and Development, Clinical Review Teams, Legal and Compliance . In addition, this individual will work closely with the Promotional ... the promotional approval process; requires collaboration with commercial legal, compliance and potentially multiple brand Clinical Review TeamLeading the planning… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …rights & wellbeing; data reliability; scientific integrity; regulatory & process compliance . Takes ownership to deliver upon near-term North America Clinical ... and IRB/REB/regulatory approvals to assure quality of the documentation files and compliance with NN SOPs, relevant regulatory requirements and ICH and GCP… 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 ... of focus include (1) the assurance of deliverable quality and process compliance , (2) effective deliverable development utilizing global and TA standards that… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director, Global Oncology Clinical Development (GOCD) Functional Excellence supports ... management and implementation planning, for GOCD non-project related initiatives. The Associate Director, GOCD Functional Excellence must have excellent verbal and… more
- Merck & Co. (Rahway, NJ)
- …and result in outcomes that demonstrate the Company's commitment to regulatory compliance . Ensures that a cross-functional team (eg Quality & Continuous Improvement ... real-time, proactive advice and guidance. Escalate potentially significant inspection findings/ compliance risks/impact to our Company Senior Management. Develops the… more
