Services:
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Continuous interaction with a customer on a current study status and all issues (scheduled meetings, reports, unscheduled communication, telephone negotiations, email);
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Maintaining and control of a project team;
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Trainings for project team members;
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Identification of potential problems and search of solutions;
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Tracking of a study status including patient enrollment status;
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Interaction with study teams and provision of strict adherence of clinical studies with the protocol, terms, budget and quality to ICH GCP/ FDA/EMA and legislation;
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Motivating of study physicians to accelerate patient recruitment;
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Checking and participation in compilation of project-specific documents (guidelines, instructions);
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Verification of monitoring reports;
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Co-monitoring;