Clinical Pharmacology Position at Cerevel

Cerevel is looking to hire a Director level role in Clinical Pharmacology/Pharmacometrics department. Interested candidates can find more details and apply for the role at following link: https://www.cerevel.com/careers/job-description/?id=998fb622-d934-4681-9edb-246ccd0a9651. Best regards Sridhar Duvvuri Job description: In this highly visible role, this individual will independently design and execute clinical pharmacology and pharmacometrics activities to support Cerevel’s portfolio. The successful candidate will have strong quantitative clinical pharmacology skills with hands-on experience in the implementation of common software tools (e.g., NONMEM, R) for PK and PK/PD analyses. This individual will act as the clinical pharmacology lead on project teams and contribute to regulatory interactions and submissions. Self-motivation, strong strategic thinking, and excellent communication skills (both verbal and writing) are required. Key responsibilities: * Responsible for planning and executing state-of-art Clinical Pharmacology program and M&S strategy to support Cerevel portfolio (early and late stage assets) * Lead quantitative clinical pharmacology activities across all phases of development to support both regulatory filings and internal decision-makings by working closely across departments (i.e. DMPK, toxicology, biology, clinical, statistics etc,) and external vendors * Represent Clinical Pharmacology on project teams and provide input in all phases of drug development, including designing and implementing dose finding strategies to ensure optimal dose and dosing regimens in clinical trials * Ensure appropriate planning and execution of data modelling/pharmacometrics activities in support of projects * Draft clinical pharmacology components of protocols, investigator's brochures, CSRs and other regulatory documents, as necessary * Manage external vendors (contracting, SOWs etc) to ensure high quality deliverables and adherence to planned timelines/budgets Required Qualifications: * 8+ years of experience in Clinical Pharmacology * Strong quantitative skills and expertise in modelling and simulation (NCA, population PK/PD modelling, literature meta-analyses, exposure-response analyses etc) * Late stage development and regulatory filing experience * Effective verbal and written communication skills are essential for the role