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...
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...
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...
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...
Associate Director, Clinical Operations Job Description Manage clinical trial activities for multiple trials... to biostatistics, medical writing, safety, regulatory affairs, and quality assurance activities. Interact closely with investigators...
Associate Director, Clinical Operations Job Description Manage clinical trial activities for multiple trials... to biostatistics, medical writing, safety, regulatory affairs, and quality assurance activities. Interact closely with investigators...
Job Title: Associate Director, Clinical Operations Job Description Manage clinical trial activities for multiple... to biostatistics, medical writing, safety, regulatory affairs, and quality assurance activities. Interact closely with investigators...
Job Description General Summary: As the Associate Director of Strategic Sourcing for Cell and Gene Therapy (CGT..., vendor quality and regulatory affairs, to align sourcing activities with production schedules, product specifications...
Job Description General Summary: The Clinical Development Associate Medical Director generalized myasthenia gravis...., Regulatory Affairs, Clinical Development Execution) for assigned studies Represents Vertex to outside medical personnel in the...
Job Description General Summary: Vertex Pharmaceuticals is looking to hire an Associate Director, North America... Markets) but more importantly across the entire organization (Medical Affairs, HR, Legal, Regulatory and Compliance teams...
We are seeking an experienced Associate Director, Scientific Communications as part of the North America Medical Affairs team to lead...Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives...
Associate Director, Global Payer Value & Access (PVA) - Vaccines will support the refinement and execution of global pricing...Job Title: Associate Director Pricing & Access - Vaccines Location: Cambridge, MA 02142 - Remote Duration: 12 Months...
We are seeking an experienced Associate Director, Scientific Communications as part of the North America Medical Affairs team to lead...Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives...
Associate Director, Global Payer Value & Access (PVA) Vaccines will support the refinement and execution of global pricing...Job Title: Associate Director Pricing & Access Vaccines Location: Cambridge, MA 02142 - Remote Duration: 12 Months...
About This Role As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will play... environment including Safety MD, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory colleagues...
and tools. Partner with regulatory and medical affairs to engage health authorities and payers on the acceptance of digital... health approaches. Ensure validation and compliance with evolving global regulatory and data privacy standards. Cross...
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...