Basic qualifications:

Scientific Degree or Equivalent Experience

1- 3 years experience of clinical study monitoring or equivalent experience in the clinical research field is an asset

Good English language written and verbal communication skills.

Advanced/expert level of MS Office (PowerPoint, Excel, Word & Outlook)

Has some level of technical expertise.

Preferred qualifications:

Masters of Science or equivalent. Advanced degree preferred but not essential


  • Fully accountable for ALL aspects of site management including ensuring completion and delivery of all local activities required to ensure high quality set up, execution and completion of studies to agreed timelines and budget.
  • Communicate progress and relevant study information or escalate issues of the study to the local study management team and other key stakeholders e.g. CRA Manager / Lead as appropriate.
  • Accountable to acquire and maintain an optimal level of knowledge in all areas to effectively perform study activities.
  • Build effective long-term collaborative relationships, and to uphold the reputation of GSK.

Contact information:

You may apply for this position online by selecting the Apply now button.

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