Director PK/PD - Pharmacokinetics - Paris

Location
Paris
Salary
Competitive
Posted
04 Jan 2019
Closes
04 Feb 2019
Ref
CS PK

This positon will offer a lot of variety including:

  • Deepen their strategic drug development expertise and broaden experience in the drug development process in general. 
  • Deepen their pharmacometric techniques with fit-for-purpose modeling approach leveraging e.g. model-based meta-analysis and E-R trial-simulations by working alongside the expert consultants.
  • To broaden and deepen their therapeutic expertise by working with a myriad of companies and drug development programs. 
  • Continue to develop -   Strategic Consulting is the largest pharmacometric consultancy organization in the world and assures that various career pathways are offered to match the ambition and personal interests of their consultants.


 

Responsibilities

  • Support projects for clients by working in teams with other Associates, expert modelers, and drug development consultants.
  • Hands on PK/PD modeling on client projects as a billable consultant.
  • May supervise project contributions of Associates.
  • May lead/coordinate company initiatives (e.g. IT, methodology, efficiency, automation, quality).
  • May act as the primary point of contact for clients and collaborate with the manager in business development.
  • Conduct quality control and quality assurance activities on model codes and reports.


 

Skills & Abilities

  • PhD, MD, PharmD in Pharmaceutical Sciences, Pharmacology, Toxicology, Statistics, Mathematics, or related field
  • 3 to 5 years of industry/consulting experience (may be combined with academic research) working in R&D, pre-clinical and clinical environments.
  • Solid experience in pharmacometrics, clinical pharmacology, pharmacokinetics, or a related discipline in a project team setting is preferred, whether in academia or industry.
  • Expertise in PK/PD modelling with strong quantitative skills
  • Advanced user of modelling software such as WinNonlin Phoenix, NONMEM, S-Plus/R
  • Experience in moving compounds through the clinical trials process and experience with various elements of clinical development and trial design and management and filings preferred.
  • Experience in a specific therapeutic area, such as oncology, cardiovascular, immunotherapy or pediatric products is of interest.
  • Proficient in spoken and written English

 

A very competitive starting salary - outstanding benefits including Holiday, Healthcare, Pension and Bonus

Please direct all questions (if necessary) to “Chris” at cswain@barringtonjames.com cswain (at) barringtonjames (dot) com alongside a copy of your CV.

 

https://uk.linkedin.com/in/christopherpswain

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