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Associate Director, Study Operations Manager - Nonclinical Toxicology at Centessa Pharmaceuticals - ApplyBlast

Associate Director, Study Operations Manager - Nonclinical Toxicology

Centessa Pharmaceuticals

1 month ago

Remote

Full Time

Director

4 applicants

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About this role

Centessa Pharmaceuticals is seeking an experienced Associate Director, Study Operations Manager to oversee day-to-day operations for toxicology and safety pharmacology studies conducted with external CROs. The role involves managing study forecasting, budgeting, data management, and quality assurance while collaborating with internal functional teams across the Orexin agonist portfolio. This position supports the company's expansion of translational science and nonclinical development capabilities.

Responsibilities

Manage end-to-end data flow between external CROs and internal teams
Initiate draft SOWs with multiple CROs for awarded studies
Monitor nonclinical toxicology and safety pharmacology studies at external CROs

Skills

Qualifications

BSc in toxicologyMSc in toxicologyBSc in pharmacologyMSc in pharmacologyBSc in a related discipline

About Centessa Pharmaceuticals

centessa.com

Company Size

51-200 employees

Founded

2021

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Centessa Pharmaceuticals is a global biopharmaceutical company that uses an asset‑centric, portfolio model to accelerate the development of innovative medicines. With a patient‑centric mission, Centessa advances programs across sleep‑wake, neurological, neurodegenerative and psychiatric disorders — notably pursuing an Orexin Receptor 2 agonist program. The company combines specialized operating subsidiaries and centralized capabilities to move preclinical and clinical‑stage assets efficiently toward regulatory approval and commercialization. Centessa partners with academic and industry collaborators to translate promising science into transformative treatment options for patients.