Drug Development Jobs in New Jersey
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Search Results - Drug Development Jobs in New Jersey
Daiichi Sankyo, Inc.-Jersey City
centered around rare diseases and immune disorders.
Summary
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...
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.-Jersey City
of optimal study design, independently develop and execute statistical analysis plan and helps in interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes...
Katalyst Healthcares & Life Sciences-Bridgewater (NJ)
experience is required.
ISS & Client experience is required.
Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
Good understanding of the clinical drug...
resume-library.com -
Daiichi Sankyo, Inc.-Newark
centered around rare diseases and immune disorders.
Summary
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...
Katalyst Healthcares & Life Sciences-South Plainfield
of policy, laws, regulations, and guidelines as they apply to U.S.
FDA for drug development and approval.
Expert understanding of drug development process and understanding of scientific content and complexities related to a project in Oncology.
Direct...
resume-library.com -
Daiichi Sankyo, Inc.-Trenton
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...
mindmatch.ai -
Tevapharm-Parsippany
adheres to departmental standards and regulatory guidelines in support of drug development, product registrations, and product marketing to meet the company’s global strategic, scientific, regulatory, and commercial goals.
The Senior Director will also...
appcast.io -
Daiichi Sankyo, Inc.-Trenton
tasks, including SDTM and collaborating with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs...
mindmatch.ai -
Pace Life Sciences-Lebanon (NJ)
About Us
Pace Life Sciences
Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP...
Daiichi Sankyo, Inc.-Trenton
strategic input into the Oncology drug development preferred.
Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of regulations, such as ICH is desirable.
Experience with CTD/eCTD preparations...
mindmatch.ai -
Pace Life Sciences-Lebanon (NJ)
About Us
Pace Life Sciences
Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP...
Daiichi Sankyo, Inc.-Newark
of optimal study design, independently develop and execute statistical analysis plan and helps in interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes...
Daiichi Sankyo, Inc.-Newark
regulatory strategic input into the Oncology drug development preferred.
• Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of regulations, such as ICH is desirable.
• Experience with CTD/eCTD...
Daiichi Sankyo, Inc.-Trenton
centered around rare diseases and immune disorders.
Summary
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...
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