Drug Development Jobs in Jersey City
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Search Results - Drug Development Jobs in Jersey City
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...
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...
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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...
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
This position is responsible for providing project management, drug development expertise to Global Project...
Daiichi Sankyo, Inc.-Jersey City
hours per week.
The program will provide opportunities interns to understand the drug development, learn about statistical applications in clinical trials, and explore/establish their interests in pharmaceutical industry for their further professional...
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...
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Tiger Analytics-Jersey City
capabilities with cloud services.
Strong understanding of the pharmaceutical/ Life Science domain, including knowledge of patient data, Commercial data, drug development processes, and healthcare data.
Collaborate with data engineers, analysts, and business...
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Daiichi Sankyo, Inc.-Jersey City
to support Sr CMC Lead. In case no Sr CMC Lead is established, take main responsibility for CMC lead. Provide operational coordination and management to drive strategies and activities for early and late phase drug development candidates within the team...
TANNER & ASSOC INC-Jersey City
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 certification...
appcast.io -
Lifelancer-Jersey City
by effectively liaising, negotiating and partnering with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development plans. The individual will direct, coordinate and implement the preparation of US...
resume-library.com -
TANNER & ASSOC INC-Jersey City
Candidates can be based out of any of these locations.
Requirements:
Major Biotech companies are seeking Medical Director/Clinical Scientist with drug development experience to join the Oncology program. The candidate should have an M.D. with board...
appcast.io -
Daiichi Sankyo, Inc.-Jersey City
to briefing documents, breakthrough therapy designation requests, orphan drug applications.
• Participate in global project team meetings (development and/or marketed products); provide regulatory support and guidance and manage day-to-day regulatory...
Daiichi Sankyo, Inc.-Jersey City
departments to strategically manage benefit-risk throughout the lifecycle of the drug. Specific responsibilities will vary depending on the stage of development of assigned projects (i.e., Phase I through commercialization).
Responsibilities
• Depending...
Daiichi Sankyo, Inc.-Jersey City
level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA submissions, working knowledge and experience in document management systems, relevant therapeutic areas, regulatory requirements, and other aspects of drug...
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