Job Description Responsibilities of the Medical Monitor: Providing Medical Leadership to the monitoring staff in the region Developing and maintaining expertise in the compounds under development and their related fields Monitoring the safety of subjects participating in the Clinical Trials Selection of Clinical Investigators Handling Serious Adverse Event Reports in accordance with the SOPs Ensuring timely distribution of IND reports to investigators and EC Review and agreement of study budgets with the sites Review of the site monitoring reports for safety Supporting the CRAs in ensuring that sites conform to GCP and SOPs Having good communication skills Additional Information All your information will be kept confidential according to EEO guidelines. J-18808-Ljbffr