- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders. **Summary:** The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery of laboratory data in ... processes and global submissions. This position provides leadership within Data Management by partnering with internal and external stakeholders to optimize… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** Under the direction of the Director/Associate Director of Clinical Management , the Senior Clinical Study Manager is responsible for the oversight and ... management of Otsuka clinical studies, including coordination with other...forecast to the Director/Associate Director.** **Establish communication flow with CRO and investigative sites to maximize compliance with study… more
- PsychoGenics (Paramus, NJ)
- Senior Project Manager **PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best ... patients. PsychoGenics is a well-established preclinical Contract Research Organization ( CRO ) that provides comprehensive preclinical testing capabilities in CNS and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …**Responsibilities:** + Study Strategy: Provides the strategic direction to Biostatistics Data Management & Data Ops for EDC, edit checks, data quality listings, ... SAP, Data Management plan; Reviews patient population and protocol compliance for...KOLs, Ad Boards for protocol development; Provides input on CRO / ARO Statement of Work and Budget; Establishes… more
- iCIMS (Holmdel, NJ)
- …team and drive our ambitious growth strategy. As a trusted partner to our CRO , you'll help shape the vision, planning, and execution across our Enterprise Sales ... work environment where everyone belongs. **Responsibilities** + Collaborate with the CRO and sales leadership team to establish vision, planning & prioritization… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …medical accountability and oversight for one or more clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1 ... eligibility questions and answers safety questions (dose modifications, discontinuations, and management of adverse events) + May participate in Site Initiation… more
- Taiho Oncology (Princeton, NJ)
- …of scientific and regulatory documents. The Associate Director of Biostatistics will have CRO oversight, management of statistical projects, and the ability to ... + Manage external biostatisticians to ensure quality performance, validate and QC CRO 's deliverables + Manage activities associated with IB updates, DSUR, PSUR and… more
- Actalent (Morristown, NJ)
- …+ At least 7 years of medical writing experience in the biopharmaceutical/ CRO industry. + Experience leading submissions for marketing approval. + Proficiency in ... organizing and communicating clinical information. + Strong organizational, time management , and project management skills. + Strong...phases of clinical trials, I-IV. + Experience in both CRO and sponsor environments. + Focus on oncology and… more
- PsychoGenics (Paramus, NJ)
- Director, EEG **PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best validated ... to help nurture their careers. + In coordination with project leaders and management , design and develop experiments to analyze EEG pattern changes induced by… more
- Danaher Corporation (Newark, NJ)
- …and ARR growth across a targeted portfolio of Biopharmaceutical, pharmaceutical and CRO /CDMO accounts. The Strategic Account Executive will report into the Senior ... teams to win SaaS business, helping some of the largest pharmaceutical and CRO / CDMO organizations in the world, accelerate their critical milestones across the… more
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