Centessa Pharmaceuticals is a clinical-stage pharmaceutical company focused on discovering, developing, and delivering impactful medicines to patients. The company specializes in rare diseases and immuno-oncology, with programs spanning from discovery to late-stage development. Led by an experienced management team, Centessa aims to rapidly advance its drug candidates through all stages of development.
Open Positions
Executive Director, Head of Toxicology
PhD in a relevant field, 15+ years of experience, and leadership experience in toxicology teams
Executive Director, Regulatory CMC
Master's degree, 15 years of experience, comprehensive understanding of FDA, EMA, and ICH CMC guidelines
Senior Director, Clinical Pharmacology
PhD in Clinical Pharmacology or related field, 8-12+ years of experience in clinical pharmacology, strong expertise in PK, PD, and PK/PD integration
Executive Director, Head of Toxicology
18+ years of experience in pharmaceutical or biotechnology R&D, PhD in Toxicology, Pharmacology, Pathology, DVM, or related discipline, Proven ability to function as an upward-facing nonclinical leader and generalist
Clinical Trial Manager
Bachelor's degree in a scientific or health-related discipline, 5+ years clinical trial management experience within an industry sponsor environment, experience managing clinical trials in CNS therapeutic development
Sr. Scientist, DMPK
Ph.D. in Pharmaceutical Sciences, 4+ years industry experience, proficiency with Phoenix WinNonlin
MSL / Sr. MSL - Northeast
PhD/MD in life sciences or related field. 2+ years medical MLO/CSL experience. Excellent communication skills. Strong understanding of clinical trials
MSL / Sr. MSL - West
Advanced degree in life sciences/related field. 2+ yrs MSL/Medical Affairs experience. Strong communication skills are crucial
Director, Program Management, CMC
10+ years of pharmaceutical industry experience, 7+ years leading CMC project/program management activities
Sr. Scientist, Drug Safety (Pharmacovigilance)
PharmD or PhD, 6+ years of experience in drug safety, prior experience in Safety Risk Assessment Meetings / Safety Review activities
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