GLP Study Director (LCMS/MS)

GLP Study Director (LCMS/MS)

Biotechnology Clinical Life Sciences

Location Adelaide, Australia

Salary £46,000 - £60,000

Contract Permanent

Reference HMAUGLPSD

Date Posted

Consultant

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Our client in Australia is looking for a highly skilled GLP Study Director to join their growing contract research clinical team based in Adelaide. The ideal candidate will have proven experience in LCMS/MS Assay Development, with working knowledge in a Study Director role within a GLP bioanalytical laboratory.

Key Responsibilities and Duties:

  • Perform Study Director / Principal Investigator roles for the bioanalytical laboratory team, reporting to the Operations Manager
  • Ensure all compliance to OECD GLP, Company guidelines and current SOPs
  • Responsible for scientific content of assigned studies
  • Establish support requirements for high level project tasks, including Project & Client Management, Sample Processing and Report Writing
  • Communicate regularly with clients on project status and progress
  • Contribute to Continuous improvement in compliance, productivity and efficiency of the laboratory team
  • Provide supervision and manage timelines internally
  • Participate in client visits/audits and regulatory audits as required

Ideal Skills and Qualifications:

  • Degree qualified, or equivalent, in a relevant scientific discipline
  • 5-10 years’ experience in LCMS/MS development in a regulated bioanalytical and Assay Development laboratory
  • Proven GLP and CRO experience; required
  • Demonstrated Study Director/Principal Investigator experience; required
  • Previous experience in communicating with clients on high level science issues as well as remaining strictly confidential
  • Experience of Watson LIMs; desirable
  • Ability to mentor, train and supervise
  • Ability to work effectively both in isolation and as part of a team
  • Ability to analyse problems, formulate effective solutions and coordinate tasks simultaneously

The company is a Contract Research Organisation specialising in providing drug development services for the pharmaceutical and biotechnology industries. You will be working in their state-of-the-art facilities based in Adelaide, Australia with Visa and relocation support provided.

If you are interested or have any questions about this role, feel free to contact Harriet (07851 246 846) at CY Partners.

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GLP Study Director (LCMS/MS)

Biotechnology Clinical Life Sciences

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