Clinical Medical Monitor

Role: Provide hands-on medical oversight for clinical programs within a biopharma setting, focusing on CNS disorders, ensuring patient safety, study quality, and compliance. Responsibilities: guide investigators on eligibility, dosing, safety, review adverse events, assess clinical data for safety signals, support site questions, and collaborate cross-functionally with clinical development, safety, biostatistics, and regulatory teams. Qualifications: MD or equivalent; experience in clinical trial safety, medical monitoring, or medical oversight; strong clinical judgment, data review skills, and familiarity with GCP standards. Preferred: CNS or relevant therapeutic area expertise. HighValue: CNS disorders, clinical trial safety, medical oversight, data assessment, investigator support. WorkSetup: remote with willingness to travel as needed.