Clinical Pharmacology, Medical Director

Location
Switzerland
Salary
On Application
Posted
19 Dec 2018
Closes
14 Feb 2019
Ref
TDCP42

This is a fantastic opportunity to oversee clinical trials and contribute to clinical pharmacology studies for an innovative and exciting biotech.

Responsibilities:

  • Lead the clinical strategy of early phases in healthy volunteers.
  • Responsible for aspects of clinical pharmacology studies on healthy volunteers such as first in human studies, PK and ADME studies.
  • Conduct and monitor clinical trials in healthy patients at early and late phases.
  • Contribution to regulatory documentation such as INDs and NDAs.
  • Determine clinical dose selection and design studies for implementation for successful study outcomes..

Requirements:

  • Educated to M.D with a focus on Clinical Pharmacology and pharmacokinetics.
  • Minimum of 3 years industry experience.
  • Experience overseeing early clinical trials in healthy volunteers.
  • Strong knowledge of PK and PK/PD analysis is desirable.
  • Previous experience working on Oncology is desirable.

If this is of interest then please contact me on tom.douglas@rbwconsulting.com or +44 (0) 1293 584 300.

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