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
Regulatory CMC strategy manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
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
Regulatory Affairs CMC Director Exciting early innovation young start up rapidly expanding to deliver phase 3 success, seeks regulatory affairs CMC Director experienced in combination products with a proven track record influencing regulators on complex innovation. Our client
Job Description SummaryAt Sandoz, our Purpose is pioneering access for patients Job Description The Head of Regulatory Data Management & Support must combine deep regulatory knowledge with strong data governance leadership and operational execution experience, with
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
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
Senior Regulatory Affairs Director Introduction to role: The Senior Regulatory Affairs Director (RAD) leads the development and implementation of global regulatory strategy for one or more products of high complexity and visibility, and may serve as
MSAT Molecule Steward Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of
Associate Principal Scientist – Peptide Development Chemistry - Pharmaceutical Sciences (PS) Location: Macclesfield, UK About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for
Job Title: Regulatory Affairs Director Location: Cambridge Salary Competitive Introduction to role: Are you ready to shape European regulatory strategy that accelerates innovative oncology medicines to patients and secures the strongest possible labels? This role puts
Company Description Bicycle Therapeutics is a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle® molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained
PE Global are currently recruiting for a Regulatory Affairs Specialist for an initial 6 month contract role with a leading multinational Consumer Health client based in Reading – hybrid (2/3 days per week in the office).
About the job Job Role: Senior Scientist, Drug Substance Location: Cambridge (Hybrid) Company Overview Our client is an emerging biotechnology company advancing a pipeline of small molecule therapeutics. The organisation works through an outsourced development model,
About the job Job Role: Senior Scientist, Drug Product Location: Cambridge (Hybrid) Company Overview Our client is an emerging biotechnology company advancing a pipeline of small molecule therapeutics. The organisation works through an outsourced development model,
Lead molecule design capability to deliver high-quality, best-in-class molecules for clinically validated targets, bringing Medicinal Chemistry, Analytical Sciences, and Structure-Based/Computational Chemistry together as an integrated unit. This is a new, strategic leadership role created to enable
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
Principal Clinical Pharmacologist, PBPK/PD Modelling Our client, a Biotech company, now seek a Clinical Pharmacologist with a strong quantitative background to support clinical development through clinical pharmacology, modelling & simulation, and pharmacokinetic analysis. This is a
Principal Clinical Pharmacometrician Our client, a Biotech company, now seek a Clinical Pharmacologist with a strong quantitative background to support clinical development through clinical pharmacology, modelling & simulation, and pharmacokinetic analysis. This hire must be resident