Our experienced Clinical Research Managers design the study together with the Biostatistician, write the study protocol, design the CRF, recruit study centres, negotiate contracts with pharmacies and study centres, apply to the Ethics Committees and the Regulatory Authorities. During the study, the Clinical Research Associate monitors the study centres and performs Source Data Validation.

According to PCG experience, the key factor in efficient Clinical Trial Management lies in efficient and timely communication. Communication to prevent, to lie ahead, to make sure things are correct and done in a proper manner. The Clinical Development Terminal, the PCG web-based project management and eCRF tool, is used in order to communicate efficiently and to be able to upload and download relevant information.

A Clinical Research Manager at PCG has at least five years of relevant experience. A Clinical Research Associate has at least two years of relevant experience.

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