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
Director, Program Management, CMC
10+ years of pharmaceutical industry experience, 7+ years leading CMC project/program management activities
Senior Director, Analytical Development, CMC Small Molecule
Advanced degree in chemistry, pharmaceutical sciences, or related field (minimum BS/MS required; PhD strongly preferred) with 15+ years of small molecule pharmaceutical industry experience
Executive Director, CMC
15 years of pharmaceutical industry experience, 8 years in CMC, strong leadership skills, and knowledge of cGMP regulations
Sr. Clinical Trial Associate (Contract)
B.A. or B.S. degree, 4+ years of experience in biotech/pharmaceutical organization, Good Clinical Practice knowledge and training, Microsoft Office proficiency
Associate Director, Clinical Operations
Bachelor’s degree, 8+ years of experience in clinical operations, and strong knowledge of clinical trial operations
Associate Director, Toxicology
PhD in Toxicology, 8+ years of nonclinical toxicology experience, and prior hands-on oversight of outsourced studies
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
Senior Director, DMPK Project Leader
Ph.D. in Pharmaceutical Sciences, Pharmacology, or a related scientific field and 10+ years of industry experience in biotech or pharmaceutical setting
(Associate) Director, Biostatistics
PhD in Statistics or Biostatistics, 10+ years of experience in pharmaceutical industry, and knowledge of CDISC standards
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