The Role Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be part
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
Location: London, UK Reporting to: Senior Director, Regulatory Science Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative cell and
Director, Regulatory Affairs EU & APAC Blackfield Associates are exclusively supporting the opportunity for a Regulatory Affairs Director to lead and expand EU regulatory capability within a global CDMO environment, with a strong focus on large
Senior Or Principal Scientist Location: London, UK Employment Type: Full-time, Permanent The Opportunity This is an outstanding opportunity for an experienced biologics scientist to play a key role in designing and advancing next-generation antibody therapeutics. You
The RoleModerna is looking for a Associate Director, CMC Regulatory Affairs-International, to join our team based in London, UK. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, governing
Associate Director – Global CMC Regulatory Strategy Location: Uxbridge, Ontario – on site 3 days a week, remote 2 days a week. Responsibilities Lead development & execution of global CMC regulatory strategies for hematology and oncology portfolios. Guide
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory
Associate Director, CMC Regulatory Affairs London, England; Oxford, England Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3
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Who Are You? An experienced Biostatistician with in-depth Bayesian analysis experience and had exposure to Chemistry, Manufacturing, and Controls (CMC) data analysis. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily
Who Are You? A Biostatistician with in-depth Bayesian analysis experience and a strong interest in Chemistry, Manufacturing, and Controls (CMC) data analysis. We welcome recent PhD graduates to also apply for this position. You are excited and
About Relation Relation is a sector defining TechBio company developing transformational medicines with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life’s most devastating
About Relation Relation is a sector defining TechBio company developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life’s most devastating