Senior Clinical Pharmacokineticist

Senior Clinical Pharmacokineticist

Quotient Sciences

Nottingham, United Kingdom

The Role

Due to our continued growth and success we have an excellent opportunity for a talented Senior Clinical Pharmacokineticist to join our Pharmacokinetics Department, within Data Sciences. You will be involved in the challenging environment of early phase clinical research and play a key role in the expansion and continuous development of our PK services.

The Senior Clinical Pharmacokineticist will also be responsible for:

  • Acting as the Lead Pharmacokineticist providing PK project oversight;
  • Provision of scientific expertise to aid in the design, conduct, and reporting of clinical studies;
  • Pharmacokinetic input to and review of Clinical Protocols and Reporting and Analysis Plans;
  • Oversight and or provision of non-compartmental pharmacokinetic analysis;
  • Providing interpretive pharmacokinetic expertise to inform dose decision making strategies, including acting as a key member of safety review committee’s;
  • Utilising modelling functionality to support emerging questions arising from clinical data e.g. Compartmental Modelling, Non-Parametric Superposition, basic PK/PD modelling;
  • Providing Pharmacokinetic, Pharmacodynamic and Clinical Pharmacological interpretive reports for inclusion in Clinical Study Reports;
  • Mentoring junior staff in a scientific capacity.

Candidate Profile

The successful candidate must have the following experience:

  • Scientific degree in a field related to Pharmacokinetics (e.g. Pharmacology, Biochemistry, Pharmaceutical Chemistry etc.);
  • Minimum of least 3-5 years of Pharmacokinetics experience;
  • Experience of WinNonlin/Phoenix®;
  • Knowledge of ICH GCP and clinical trials.

The following additional experience would be advantageous in this role:

  • Previous project lead experience e.g. scheduling and resource management;
  • Line management, or experience of mentoring junior staff;
  • Experience in a range of clinical studies e.g. of First in Human , DDI, Drug Product Optimisation, Bioequivalence and ADME;
  • Familiarity with a combination of the following - regulatory bioanalysis, drug metabolism, formulation development, human dose prediction/justifications, PBPK, and pre-clinical safety data utility in the clinical setting;
  • Utilisation of modelling and simulation techniques supporting clinical strategy decision making;
  • Familiarity with related software/processes e.g. SAS®, CDISC terminology, statistical methodologies etc.;
  • Experience of working with Data Management, Statistical Programming, Statistics and Medical Writing departments.

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© EuroJobsites 2020

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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