Clinical Pharmacokinetics Consultant

Location
Home-based
Salary
On application
Posted
21 Apr 2021
Closes
21 May 2021
Ref
TDPK3893
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

We are currently collaborating with a growing CRO that are looking to develop their pharmacokinetics expertise in Europe. This opportunity will require you to act as a study lead for all pharmacokinetic aspects of phase 1 studies for a dedicated sponsor. You will have the chance to work with a highly experienced team of clinical pharmacology experts to provide drug development consultancy.

Responsibilities:

  • Write and review the pharmacokinetic reports and discuss with the client.
  • Provide scientific input into the design of clinical pharmacology studies.
  • Contribution to regulatory documents including IBs and CTDs.
  • Oversee the performance of non-compartmental pharmacokinetic analysis and ensure it is completed in accordance with ICH-GCP guidelines.
  • Act as project manager for clinical pharmacology studies which will involve leading a team of scientists to ensure timelines are met.

Requirements:

  • Educated to BSc with a minimum of 2 years industry experience in the pharmacokinetics field.
  • Experience contributing to clinical pharmacology studies with a focus on PK aspects.
  • Understanding of regulatory guidelines for clinical studies.
  • Experience using Phoenix WinNonlin for non-compartmental analysis.
  • Previous experience as a project manager would be beneficial.

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