Proclinical

Lead world-class drug substance development from concept to GMP production as a Senior Principal Scientist. This Palo Alto-based role requires a Ph.D. with 8+ years of process chemistry expertise, including CDMO management and cGMP manufacturing. You will provide technical leadership for outsourc...

Join our client as a Senior QA Specialist (CMO Oversight) in Uxbridge, UK. You will ensure cGMP compliance and manage quality systems for commercial drug products at external vendors. This role requires strong regulatory knowledge (FDA/EMA) and experience in pharmaceutical quality oversight. Appl...

Join a leading pharmaceutical company as a Key Account Manager in Stuttgart. Drive patient identification for rare liver diseases (PFIC/PBC) by building regional networks with healthcare professionals. This role requires rare disease expertise, key account management skills, and a willingness to ...

Lead early-stage lentiviral vector process development and analytical innovation in Brabant Wallon. This strategic role focuses on platform building, technical de-risking, and scalable bioreactor design. Requires a PhD/MSc with viral vector bioprocess leadership and CDMO experience. Build the tec...

Join our Boston team as a Veeva Clinical Business Administration Specialist. You will optimize Veeva Vault Clinical systems, providing crucial user support and driving process improvements. The role requires expertise in eTMF/CTMS, system validation, and clinical trial processes. This is a key op...

Join a dynamic team in London as a Clinical Services Manager. You will promote innovative diabetes management products, providing education to healthcare providers and patients. The role requires strong clinical credentials, experience with insulin pumps, and excellent communication skills. This ...