Job Title: Associate Director Global Regulatory Affairs Location: Cambridge, MA 02142 Duration: 06+ Months...: knowledge of US Regulatory Affairs Recommended experience: 0-3 years for Associate level, 4-7 years Intermediate level, and 8...
Job Title: Associate Director Global Regulatory Affairs Location: Cambridge, MA 02142 Duration: 06+ Months Hybrid... of US Regulatory Affairs Recommended experience: 0-3 years for Associate level, 4-7 years Intermediate level, and 8+ for Senior level...
of what is possible in order to bring life-changing therapies to patients worldwide. The Director Global Regulatory Affairs, Neuroscience... within Global Regulatory Affairs and Takeda R&D. How you will contribute: The Director will be responsible for increasingly...
Job Description General Summary: The Associate Director, CMC Regulatory Affairs, Biologics executes multi-product... global regulatory CMC strategies for investigational and marketed products, with a focus on biologics. This role leads the...
Rare Diseases, Regulatory Affairs Ad Promo function for the United States, with additional duties in Canada. Manage... points Ensures regulatory compliance while effectively managing business risks Understands global promotional strategies...
As Associate Director, Global Regulatory Strategy / International Regulatory Affairs, reporting to the Senior Director... better, longer. For more information, visit us at . About the Role Associate Director, Global Regulatory Strategy - International...
Clinical Development, NA Field Medical Affairs, HEOR, Market Access, Marketing, Regulatory Affairs, and the Global Medical... Affairs Lead, the Associate Scientific Director will ensure that scientific and medical strategies are strategically aligned...
Job Description General Summary: The Advertising Promotion Associate Director is responsible for providing... Regulatory Affairs Advertising and Promotion representative on program and other cross-functional teams May serve as Chair...
(Associate Director) - Global Manufacturing Science GMSci Drug Product (DP), you will provide technical expertise within the... Regulatory Affairs. SME for Takeda drug product manufacturing organization and network. In depth and broad understanding...
Medical Director for Hematologic Oncology, the Associate Medical Director will provide a single medical affairs voice in the... Associate Medical Director will be responsible for medical activities including congress activities, coordinating cross-company...
across early- and late-stage clinical development, regulatory strategy, and medical affairs Expertise in key therapeutic areas...Job Description: Who Are Prescient? We are a specialist, strategic partner to global biopharma companies...
Associate Director, Field Medical Excellence & Training will lead the development and execution of standardized systems... companies, today we are listed on the Taipei Exchange (6446) and are expanding our global presence with operations in the...
About This Role: As the Associate Director of Marketing for Rare Disease, you will play a pivotal role in advancing... partners and internal functions such as Patient Advocacy, Corporate Affairs, Field Force, Medical, Legal, Regulatory, Finance...
Associate Director, Commercial Engagements & P2P Strategy, offers a unique opportunity to shape Takeda's first commercial... with internal cross-functional stakeholders (Marketing, PRT, Medical Affairs, Legal, Regulatory, Ethics & Compliance) to ensure the...
Title: Associate Director, Biostatistics Company: Ipsen Innovation (SAS) About Ipsen: Ipsen is a mid-sized global... and regulatory requirements. In addition to managing internal teams and external partners, the Associate Director plays a pivotal...
. Responsible for understanding the regulatory requirements related to the clinical studies and global drug development... Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie...
and regulatory filings; Author and/or provide senior review of clinical protocols, medical affairs and regulatory documents/filings... and implementation. Liaise with relevant stakeholders in clinical, regulatory, and commercial to coordinate and align biomarker...
processes and training and ensure alignment with global processes and regulatory requirements and expectations. Drive the..., ensuring alignment with global processes and regulatory requirements. Create and deliver training solutions to support the...
Job Description Reporting to the Associate Director of Product Development, this role will focus on the design..., Regulatory Affairs, Clinical Development, Analytical, and Manufacturing functions, as required. The position will be located...