Full-time Posted June 02, 2026
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Job Description

Job Description

  • You are responsible for managing biomarker studies as part of clinical trials according to the regulatory requirements;
  • You carry out consultations and provide operational input into quotes/proposals to ensure capabilities and client needs are aligned;
  • You check the scope of work and budget accurately to achieve client expectations at all times;
  • You define project milestones and check project performance against protocol, from signed contract to invoice paid;
  • You control if the project is conducted in accordance with set global standards and procedures;
  • You control the budget of assigned studies;
  • You complete and accurate study files to pass prevailing regulatory inspections;
  • You support sponsor and internal audits.
  • Qualifications

  • You have at least a Master’s degree in Biochemistry/ Life Sciences or a Bachelor degree in Biochemistry/Life sciences along with signif...
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