Daiichi Sankyo Edison, NJ Jobs

1 - 10 of 42 Jobs
Clinical Supply Operations Intern
Daiichi SankyoHealth & Medical
Edison, NJ
We are currently seeking a Clinical Supply Operations Intern. This position will input data to support ongoing Clinical Programs; work with supervisor to assure availability of drug product, and maint
from dsi.comYesterday
Manager, QA IMP-GMP
Daiichi SankyoTech Quality Assurance
Edison, NJ
The incumbent oversees the implementation of quality systems and GMP compliance programs for Investigational Medicinal Product (IMP), collaborates on cross-functional teams, and consults on work prepa
from dsi.com3 days ago
Director, Clinical Trial Info Disclosure
Daiichi SankyoHealth & Medical
Edison, NJ
This position provides strategic and operational expertise to the organizations commitment to disclose clinical trial and result information according to local regulations and the clinical trial data
from dsi.com4 days ago
Manager, Regulatory Affairs Strategy
Daiichi Sankyo
Edison, NJ
This position is responsible for assisting with the preparation, coordination and monitoring of routine US regulatory submissions (e.g., IND/NDA submissions, Annual Reports, Investigator Brochures, IN
from dsi.com8 days ago
Senior Scientist Clinical Pharmacology
Daiichi SankyoHealth & Medical
Edison, NJ
The primary responsibilities of this position are to design, conduct and interpret Phase 1 studies with supervision, support implementation of clinical pharmacology operations for Phase 2/3 studies, a
from dsi.com25 days ago
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Regional QA The Americas Intern
Daiichi SankyoIntern / New Graduate
Edison, NJ
Assist in Regional GMP Quality Assurance with audit proposals and tracking, preparing reports and presentations, applying Quality Audit metrics from the site data, preparing risk assessments and suppo
from dsi.com25 days ago
Associate Director Biostatistics
Daiichi SankyoHealth & Medical
Edison, NJ
Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with m
from dsi.com26 days ago
Director, Regulatory Info Mgmt
Daiichi SankyoTech Management
Edison, NJ
Responsible for all Regulatory Information Management and Records Management activities for the DS Regulatory West Development business. Operates as the Regulatory Information Management expert. Respo
from dsi.com30+ days ago
Assoc Dir Clinical Operations
Daiichi SankyoHealth & Medical
Edison, NJ
Lead execution of global or local clinical studies, in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU
from dsi.com30+ days ago
CMC Management & Operations Intern
Daiichi SankyoOperations
Edison, NJ
Facilitates coordination of global CMC development teams. Assists with CMO management. Works with supervisor to prepare CMC timelines, budgets, support of issue resolution and Project maintenance. Res
from dsi.com30+ days ago

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