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Drug Development Jobs in Massachusetts

1 - 15 of 109
1 - 15 of 109
Search Results - Drug Development Jobs in Massachusetts
apartmentQilu PharmaceuticalplaceBostonevent_available
About the Role The Chief Scientific Officer - Early Drug Development will formulate and lead the company's global early-stage R&D strategy, establishing the R&D roadmap from target validation to proof-of-concept (POC). Responsibilities  •  Lead...
apartmentTakeda PharmaceuticalplaceBostonevent_available
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...
apartmentThe Fountain GroupplaceCambridgeevent_available
Overview: Looking for a strong Clinical Regulatory Writer with direct pharmaceutical industry experience, specifically someone who has authored regulatory documents throughout the drug development lifecycle. Must-Have Experience Hands-on...
apartmentTakeda PharmaceuticalplaceBostonevent_available
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...
apartmentSoTalentplaceBostonevent_available
to drive labeling strategy and execution for multiple drug development programs across US and EU markets. This role leads cross-functional teams to develop, maintain, and implement product labeling content, ensuring compliance with global regulatory...
apartmentTakeda PharmaceuticalplaceCambridgeevent_available
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...
apartmentTakedaplaceCambridgeevent_available
of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Who has a proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams...
apartmentTakeda PharmaceuticalplaceCambridgeevent_available
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...
apartmentGForce Life SciencesplaceCambridgeevent_available
and/or established organic chemistry techniques and innovative approaches to address synthetic challenges, playing a pivotal role in our drug development pipeline. Qualifications:  •  Ph.D. (1-3 years of experience) or M.Sc (5+ years of experience) with strong...
apartmentTakeda PharmaceuticalplaceBostonlanguagemindmatch.aievent_available
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...
apartmentTakeda PharmaceuticalplaceBostonevent_available
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 issues...
apartmentZenith LifeScienceplaceBostonevent_available
degree in an appropriate discipline.  •  Significant medical writing experience in the pharmaceutical industry or CRO.  •  Ability to advise and lead communication projects.  •  Understand drug development and communication process from development, launch...
apartmentTakeda PharmaceuticalplaceBostonlanguagemindmatch.aievent_available
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 issues...
apartmentSciProplaceBostonevent_available
that integrates multi-modal biological data, advanced analytics, and clinical insights to accelerate drug development and improve patient outcomes. This is a high-impact leadership opportunity to define and scale the product organization at the intersection...
apartmentTakeda PharmaceuticalplaceBostonevent_available
medicine. Expert knowledge of device development, registration and maintenance requirements with experience in championing innovation in technical areas. Comprehensive understanding of biomarker strategies and implications for drug development. Demonstrated...
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