Medical Monitor

at  Alimentiv

This role is intended to provide unbiased medical guidance to clinical sites and internal and external study operations teams. The medical monitor provides therapeutic and compound training, medical guidance on protocol compliance, ensures medical congruency at subject and study level and oversight of coding of medical terms. The medical monitor supports clinical safety, project, and data management by reviewing critical study materials at study start up stage and data listings though the study duration. The medical monitor may also assist with reviewing the interim or final data sets and the writing of the final study report. The medical monitor provides regular communication to the medical team (including medical teleconferences), and interfaces with the internal cross functional teams as well as sponsor medical groups throughout the study.

KNOWLEDGE

• Maintain a thorough working knowledge of protocol(s) and the current Investigator Brochure(s) with particular attention to those aspects relating to safety data involving human subjects.

QUALIFICATIONS

• Must have a medical degree. Strong understanding of drug development process, ICH and Good Clinical Practices, and 4-6 years of related experience with substantial on-going job-related training. Strong written and verbal communication and presentation skills, enabling effective interactions with team members within Alimentiv, client company personnel and prospective sponsors.

Please refer the Job description for details