To provide scientific expertise to development design conduct and analysis of POC clinical trialsprojects in accordance with Clinical Development plans agreed by the Project Team To contribute to and review trial related documentation such as eCRF informed consent form medicalstatistical supervision
Member of the licensing team contributing to financial and scientific valuationsMAIN TASKS RESPONSIBILITIES Identify new growth opportunities and areas of innovation that can transform and further build the Endocrinology and Fertility franchises of Merck Serono for the future Drive
To oversee the conduct of clinical trials within the agreed time‑scale To represent Global Clinical Monitoring CM on the Trial Team for insourced or outsourced trials and operate as central communication channel between Trial Team and the Clinical Monitoring DepartmentFor outsourced
