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