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Position Details
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...