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Study Director - LCMS

Job Title: Study Director - LCMS
Contract Type: Permanent
Location: North Yorkshire, England
Industry:
Salary: £35000 - £45000 per annum + Benefits
Start Date: ASAP
Reference: J904949_1582802833
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Job Published: February 27, 2020 11:27

Job Description

Role: PK Study Director LC-MS

Location: Yorkshire

Salary: Highly competitive

Russell Taylor Group has a fantastic opportunity for a Study Director who specialises in bio-analysis, LC-MS / PK studies. You will also have experience in LCMS Method Development / Validation and worked within a GLP and GCP environment. We are accepting applications now but not for long so please apply to avoid disappointment!

Role:

  • Responsible for different study types (validation, analytical and equipment studies)
  • Supervise staff performing the lab work, any draft studies and validation
  • Responsible for reviewing all study data for GLP / GCP compliance
  • You will transfer all study data into reports
  • Performing quantitative analysis using LC-MS and multiplied immunoassays
  • Provide assistance in the technical, scientific, practical, GLP / GCP compliance throughout the business
  • Evaluate and establish operation of LC-MS platforms and supporting equipment
  • Maintain and build upon industry leading processes to ensure the highest quality and efficiency is achieved

Person:

  • A minimum of 2 years' appropriate experience in clinical and/or preclinical bioanalysis laboratory.
  • Strong background in the development of LC-MS bioanalysis methods in support of PK and Biomarkers
  • Strong background in support of regulatory validation and sample analysis studies
  • Experience in a regulatory environment and in directing regulated studies, experience working with GLP and GCP
  • Experience in a client facing role with the ability to provide high level advice and guidance to clients
  • Experience of driving the introduction of new instruments, processes and best in class practices
  • Proven Industry Experience in Study Directing - Previous Study Directing experience within a GCP/GLP laboratory is essential. Individuals with significant LC-MS/MS bioanalysis experience looking to step up will also be considered.

Keywords; Study Director, LC-MS, GLP, GCP, bio-analysis, method validation, method development,

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