5 days ago Be among the first 25 applicants Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Astrix Technology. Drug Safety Physician Clinical Chicago, IL, US Pay Rate Low: 180000 | Pay Rate High: 250000 Added - 19/05/2025 Apply for Job At Astrix, we're expanding our team to support a diverse range of clients across various industries. We're seeking talented Drug Safety Physicians to join us! Our partners range from emerging biotech firms to established pharmaceutical companies, all seeking professionals who can bridge scientific insights with clinical application. Opportunities are available both remotely and on-site throughout the country! Location: Central Region (Remote with Onsite Collaboration as Needed) Salary Range: $180,000 – $250,000 (based on experience and qualifications) Key Responsibilities Conduct medical reviews of individual case safety reports (ICSRs) to assess seriousness, expectedness, and causality. Contribute to the preparation and review of aggregate safety reports, including Development Safety Update Reports (DSURs), Periodic Safety Update Reports (PSURs), and Risk Management Plans (RMPs). Participate in signal detection activities and safety data analysis to identify potential safety concerns. Provide medical input into clinical trial protocols, investigator brochures, informed consent forms, and other clinical documents. Collaborate with cross-functional teams to integrate safety considerations into product development. Support the preparation of safety sections for regulatory submissions and responses to health authority inquiries. Stay current with global pharmacovigilance regulations and guidelines to ensure compliance and best practices. Qualifications Medical degree (MD or equivalent) required; board certification in a relevant specialty is preferred. Minimum of 3 years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotechnology industry. Strong knowledge of global pharmacovigilance regulations and guidelines (e.g., FDA, EMA, ICH). Preferred Qualifications Experience in oncology, infectious diseases, or other specialized therapeutic areas. Familiarity with signal detection methodologies and tools. Experience in authoring and reviewing safety-related regulatory documents. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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