- Merck & Co. (Rahway, NJ)
- …Drug Development, Logistics, Multiple Therapeutic Areas, Process Optimization, Publications Management , Regulatory Compliance, Risk Management , Sourcing ... internal and external to GCS and serves as the lead GCS spokesperson at clinical and development...with stakeholders at various levels, including cross-functional teams, senior management , external vendors, and clinical sites. Strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …MD, will lead the development and implementation of integrated project/product risk management strategies aimed at achieving the optimum benefit- risk ... a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management , Biostatistics, Pharmacology, and other… 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 ... a difference? The Position The Patient Safety, Compliance & Operational Excellence Lead is responsible for driving efficiency, quality, and innovation across US… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …data acquisition, validation, and reconciliation, study data protection, operational metrics, and clinical trial quality and risk management reporting ... to manage and coach people, and the capability to lead multiple projects concurrently are crucial for this role....and reconciliation reports, study data protection, operational metrics, and clinical trial quality and risk management… more
- Merck & Co. (North Wales, PA)
- …for our patients, partners, and colleagues.As a Technical Product Manager for the Compliance, Risk , Quality, & Vendor Management product you will spend a lot of ... across the organization. Candidate will be accountable for the entire Compliance, Risk , Quality, & Vendor Management product from the prioritization and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigations Lead is responsible for providing quality oversight over the...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …signal, epidemiological data, and regulatory requirement synthesize into a coherent risk management strategy.Represents the CSPV department as subject matter ... cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the daily strategic initiatives… more
- Merck & Co. (Rahway, NJ)
- …Project Strategy, Regulatory Compliance, Regulatory Requirements, Resource Stewardship, Results-Oriented, Risk Management {+ 5 more}Preferred Skills: Current ... Job DescriptionThe Director, Master Data Management (MDM) will lead a centralized...(AQIP), Academic Quality Improvement Program (AQIP), Adaptability, Budget Development, Clinical Supply Chain Management , Clinical … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and external vendors/contractors Ensure seamless operations and timely delivery of safety data Risk Management Act as the primary point of escalation for ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...resourcing for case processing. This role leads the Case Management Activities and oversight of case Intake, Triage and… more
- Organon & Co. (Plymouth Meeting, PA)
- …to internal and external cross-functional teams and vendor teams, and manage the clinical study team to develop and implement risk mitigation strategies and ... TMED Operations. The CTM will support the TMED Operations Lead to plan and execute studies including, but not...operations + ICH/GCP + Clinical research + Clinical development + Vendor selection and management … more
