Drug Development Jobs in New Jersey
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Search Results - Drug Development Jobs in New Jersey
Daiichi Sankyo, Inc.-Jersey City
focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Sr Director GPM&L is accountable for delivering an integrated drug development strategy and tactical plan...
PMV Pharmaceuticals, Inc.-Princeton (NJ)
PMV Pharma is seeking an exceptional Director of CMC Project Management to oversee and manage Chemistry, Manufacturing, and Controls (CMC) activities for our drug development projects. The ideal candidate will have extensive experience...
mindmatch.ai -
Daiichi Sankyo, Inc.-Newark
focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Sr Director GPM&L is accountable for delivering an integrated drug development strategy and tactical plan...
Katalyst Healthcares & Life Sciences-Florham Park
products, FDA standards for quality, data requirements and knowledge of the NDA review process.
Experience with small molecule drug development, late-stage drug development, and commercial stage programs is a plus. (knowledge of pharmaceutical development...
resume-library.com -
Daiichi Sankyo, Inc.-Trenton
focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Sr Director GPM&L is accountable for delivering an integrated drug development strategy and tactical plan...
Daiichi Sankyo, Inc.-Jersey City
supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization...
Cost Management Incentives Inc-Jersey City
Manager, Project Management is responsible for providing support to regional and global Drug Safety Pharmacovigilance (PV) projects. Projects include global marketing application and clinical development programs. Responsibilities include supporting...
resume-library.com -
Daiichi Sankyo, Inc.-Jersey City
high quality data.
• Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre...
Taimei Technology-Princeton (NJ)
objectives and support seamless project delivery.
• Monitor industry trends and client-specific challenges in drug development to proactively address client needs and identify new opportunities.
• Track, analyze, and report key performance indicators (KPIs...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
high quality data.
• Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre...
Tevapharm-Lake Hiawatha
and regulatory guidelines in support of drug development, product registrations, and product marketing.
The Senior Director will also:
• Offer clear leadership and extensive accountability, strategic vision, and planning direction at the global function level...
appcast.io -
Daiichi Sankyo, Inc.-Trenton
supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization...
Katalyst Healthcares & Life Sciences-South Plainfield
issues to CT3 leadership as appropriate.
Requirements:
Develop working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles.
Gain exposure to all phases of drug development.
Assist in handling...
resume-library.com -
Daiichi Sankyo, Inc.-Newark
high quality data.
• Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre...
TANNER & ASSOC INC-Jersey City
Candidates can be based out of any of these locations.
Requirements:
Major Biotech companies are seeking Medical Directors/Clinical Scientists with drug development experience to join the Oncology program. Candidates should have an M.D. with board...
appcast.io -
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