This is what you will do: The Associate Director is a cross-functional leader responsible for overseeing Alexion...'s external clinical manufacturing operations for small-molecule, biologics, and gene therapy drug substance and drug product...
Job Description General Summary: The Manufacturing Process & Technical Quality Associate Director is accountable... functions and commercial supply chain to drive manufacturing and compliance continuous improvements throughout the clinical...
Cambridge, US; London, United Kingdom | full time | Job ID: 9862 About the role Lead Global Clinical Supply... Strategies That Make a Difference. Orchestrate portfolio-level supply strategies for global clinical trials, ensuring patients...
closely with the Sr. Clinical Trial Manager and Clinical Operations Team, the Clinical Trial Associate (CTA) contract position... standard operating procedures (SOPs). The CTA will support the Sr. Director of Clinical Operations and Clinical Trial Managers...
of breakthroughs. The Associate Director – Territory Operations Manager (AD-TOM) is a regional expert supporting Patient Operations... and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality...
Associate Director/Director level. As a key member of the core product development team, you will have the opportunity.... In advancing several product candidates into clinical stage, CRISPR Therapeutics will offer the right individuals the opportunity...
Job Description Associate Director, Data Science - Neuroscience Biomarker Discovery Our Company’s Data, AI & Genome... Sciences Department in Cambridge, MA is seeking an Associate Director, Data Science - Neuroscience Biomarker Discovery...
Job Description Associate Director, Data Science - Neurodegenerative Causal Biology Our Company’s Data, AI & Genome... Sciences Department in Cambridge, MA is seeking an Associate Director, Data Science - Neurodegenerative Causal Biology...
and other presentations . About the Role Associate Director, Regulatory Affairs CMC As the Associate Director, Regulatory Affairs CMC..., reporting to the Senior Director, Regulatory Affairs CMC, you will be responsible for developing and executing the CMC...
Job Description The Product Quality Associate Director is accountable for end-to-end quality oversight of small... molecule program(s) throughout clinical development, commercialization, filing, approval, launch, and post-approval lifecycle...
Job Description General Summary: The Associate Director, GMP Operational Quality is responsible for quality... with cross-functional partners such as analytical and process development, clinical and commercial QC, and manufacturing...
Job Title: Associate Director, Drug Substance Location: Cambridge, MA About the Job Are you ready to shape the... Sciences, Process Engineering and Clinical Manufacturing/External Technologies, define the control strategy for the...
from chronic management to single-course gene editing medicines. Position Summary: The Associate Director, Regulatory CMC... subsidiary of Eli Lilly & Company, is a clinical-stage genetic medicines company established with a mission to solve the global...
Research Project Management Lead (Associate Director) About This Role We are seeking an experienced project..., and manufacturing functions to manage and execute integrated project plans for IND-enabling activities, regulatory filings, and clinical...
Job Description General Summary: As Associate Director of Cell & Gene Therapy Forecasting, you will lead global... to shape commercial strategy, and ensure the integration of the latest market, competitive, and clinical intelligence...
to collaborate closely with the Research, Process Development, Manufacturing, Quality, Regulatory functions to develop and deliver... products to the clinical. The ability to work in a matrix team environment is essential. As a member of dynamic and diverse...