Medical Monitor Contractor

Working remotely, the Medical Monitor Contractor will oversee clinical trial safety, ensure compliance with regulatory standards, and collaborate with cross-functional teams on medical monitoring activities. Key responsibilities Manage and review clinical trial safety data and reports Ensure adherence to regulatory requirements and company policies Collaborate with clinical teams to address safety concerns and provide medical expertise Required qualifications Medical degree (MD or equivalent) with relevant clinical experience Experience in clinical trial monitoring or medical oversight Knowledge of regulatory guidelines and Good Clinical Practice (GCP) Eligibility to work in the United States without visa sponsorship Strong understanding of clinical research processes and safety monitoring