Drug Development Jobs in Connecticut
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Search Results - Drug Development Jobs in Connecticut
SciPro-Ridgefield (CT)-appcast.io-
development and bringing new medicines to market. It’s a highly collaborative environment where scientific impact and long-term drug development really matter
Key Responsibilities:
• Execute tissue processing to prepare high-quality samples for analysis...
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Takeda Pharmaceutical-Boston-tdrct.com-
and inform COA measurement strategies to support development, post-authorization and commercial research activitie ngs across the lifecycle of drug development.
• Contribute to the strategy development and generate evidence for COA-based support tools...
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SciPro-Ridgefield (CT)-
stage clinical development and bringing new medicines to market. It’s a highly collaborative environment where scientific impact and long-term drug development really matter
Key Responsibilities:
• Execute tissue processing to prepare high-quality...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
with strong practical experience with global HA requirements, beyond EU/US. who has an understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Who has a proven ability to understand...
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Pfizer-Groton (CT)-dejobs.org-
for oncology programs.
**ROLE RESPONSIBILITIES:**
+ Represent Clinical Pharmacology on Clinical Sub Team and Development Team.
+ Participate in the implementation of model-based drug development using quantitative approaches to address complex...
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3 similar jobs: New York, Collegeville, Cambridge
Takeda Pharmaceutical-Cambridge-tdrct.com-
management within the global project team. The QCP role works in partnership with the pharmacometrics lead to drive a MIDD path within each project.
• Leads strategic, scientific, and operational aspects of multiple drug development projects with a high...
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Pfizer-Groton (CT)-dejobs.org-
Participates in implementing model-based drug development using quantitative approaches to address scientific questions arising during drug development.
+ Provides non-compartmental analysis of PK data and executes appropriate PK/PD analyses...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.
• Analyze...
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Pfizer-Groton (CT)-dejobs.org-
leading trials
+ Experience across multiple phases of clinical development and across drug classes in oncology
+ Experience in leading NDA, BLA or MAA
Candidate demonstrates a breadth of diverse leadership experiences and capabilities...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.
• Analyze issues with attention to detail.
• Base regulatory...
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Pfizer-Hartford-dejobs.org-
health economics and / or market access & pricing and related fields.
+ In depth understanding of pricing and access dynamics is required
+ Experience in Hemato-oncology is preferred
+ Knowledge and experience in drug development. Strong...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
Quality Assurance can be considered.
• Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development...
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Pfizer-Groton (CT)-dejobs.org-
to be an internal subject matter expert in their therapeutic area and in clinical drug development.
They may assume responsibility for other clinical leadership opportunities in support of the Obesity portfolio. This may include responsibilities for trial...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
Preferred experience in reviewing, authoring, or managing components of regulatory submissions.
• Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post-marketing a plus.
• Understand...
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Takeda Pharmaceutical-Cambridge-tdrct.com-
in reviewing, authoring, or managing components of regulatory submissions.
• Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post-marketing a plus.
• Understand and interpret complex...
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