NONMEM Users Network Archive

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Clinical Pharmacology Position at Cerevel

From: Sri Duvvuri <PKscientist>
Date: Mon, 8 Mar 2021 15:24:02 +0000

Cerevel is looking to hire a Director level role in Clinical Pharmacology/P=
harmacometrics department. Interested candidates can find more details and =
apply for the role at following link:

https://www.cerevel.com/careers/job-description/?id=998fb622-d934-4681-9e=
db-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 Cer=
evelís 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, st=
rong strategic thinking, and excellent communication skills (both verbal an=
d writing) are required.

Key responsibilities:

  * Responsible for planning and executing state-of-art Clinical Pharmaco=
logy 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-mak=
ings 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 t=
rials
  * Ensure appropriate planning and execution of data modelling/pharmacom=
etrics activities in support of projects
  * Draft clinical pharmacology components of protocols, investigator's b=
rochures, CSRs and other regulatory documents, as necessary
  * Manage external vendors (contracting, SOWs etc) to ensure high qualit=
y 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-respon=
se analyses etc)
  * Late stage development and regulatory filing experience
  * Effective verbal and written communication skills are essential for t=
he role


Received on Mon Mar 08 2021 - 10:24:02 EST

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