To support a clinical-stage biopharmaceutical company, the remote Safety Physician will develop patient-centric risk management strategies, oversee safety activities for investigational compounds, and manage safety issue responses while ensuring compliance with regulatory requirements. Key responsibilities Develop proactive risk management strategies and oversee benefit-risk assessments for investigational products Plan, manage, and analyze Safety/Pharmacovigilance activities for study medications, including serious adverse event reviews Provide clinical support for regulatory submissions and lead safety data review meetings with clinical teams Required qualifications Medical degree with extensive clinical or research experience At least 10 years of experience in Pharmacovigilance and Risk Management within the pharmaceutical or biopharma industry Significant knowledge of clinical development regulations and experience with regulatory submissions Proven leadership and project management skills, preferably with experience in Oncology Strong understanding of ICH, GCP, and FDA/EMA guidelines and regulations