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    Senior Scientific Director - Boston, MA, United States - Cerevel Therapeutics

    Cerevel Therapeutics
    Cerevel Therapeutics Boston, MA, United States

    2 weeks ago

    Default job background
    Full time
    Description
    Cerevel Therapeutics is dedicated to unraveling the mysteries of the brain to treat neuroscience diseases.

    We are tackling neuroscience diseases with a differentiated approach that combines expertise in neurocircuitry with a focus on receptor selectivity.

    Our portfolio of pre-commercial neuroscience assets targets a broad range of central nervous system (CNS) disorders, including schizophrenia, epilepsy, Parkinson's disease and substance use disorder.

    Headquartered in the Greater Boston area, we are bold thinkers, deep experts, resilient pathfinders, and transparent partners who push the boundaries of scientific understanding to unlock breakthrough CNS therapies that have real impact on people's lives.

    In this highly visible role, this individual will independently and implement model informed drug development (MIDD) activities and help optimize drug development projects in Cerevel's portfolio.

    Ideal candidate will be a leader in Pharmacometrics and 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 own the pharmacometrics strategy across the portfolio and has a successful track record of contributing to regulatory interactions and submissions.

    Self-motivation, strong strategic thinking, and excellent communication skills (both verbal and writing) are required.
    Responsible for planning and executing MIDD and pharmacometrics strategy to support Cerevel portfolio
    Lead M&S activities across all phases of development to support both regulatory filings and internal decision-makings by working closely across departments (i.e. Represent Pharmacometrics, by working closely with clinical pharmacology leads 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
    Develop Pharmacometrics group and mentor junior colleagues on population analysis methodology
    Contribute Pharmacometric expertise to regulatory strategy
    Manage external vendors (contracting, SOWs etc) to ensure high quality deliverables and adherence to planned timelines/budgets

    or equivalent training in pharmacokinetics, Pharmacometrics, PKPD modelling or related disciplines with 12+ years of experience
    Expert level skills and expertise (or ability to manage) in modelling and simulation activities (NCA, population PK/PD modelling, literature meta-analyses, exposure-response analyses etc)
    Late stage development and regulatory filing experience

    Cerevel is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by applicable law.

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