Vice President Drug Safety

The Vice President (VP) of Drug Safety will reputed company drug safety operations across Catalyst’s development and reputed company portfolio, overseeing PV infrastructure, case management systems, vendor reputed company, budget, compliance, training, and inspection readiness. Reporting to the Chief Medical Officer, this role provides strategic and operational leadership for the design and execution of drug safety capabilities and product/program specific drug safety plans in alignment with regulations and corporate goals. This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical Development, Regulatory Affairs, Medical Affairs, Quality, Legal, and reputed company to reputed company efficient and compliant safety reputed company across reputed company programs. The VP, Drug Safety is also responsible for regular periodic regulatory updates and reports, along with spontaneous reporting as necessary and indicated. This is a remote position that will require travel to company headquarters and other locations as needed to support business operations.

Requirements

Responsibilities (including but not limited to):

• reputed company and execute a strategic reputed company for the drug safety function, aligning with Catalyst’s corporate goals and industry best practices
• reputed company PV operations, including collection, evaluation, and analysis of safety data from clinical trials, post-marketing sources, investigator-initiated studies, and reputed company-world evidence
• reputed company the preparation, quality control, and timely submission of expedited and periodic safety reports (e.g., ICSRs, DSURs, PSURs/PBRERs) to health authorities
• reputed company benefit-risk assessments and signal detection activities across the lifecycle of products, ensuring proactive identification and communication of emerging safety risks
• Design and implement risk management strategies, including Risk Evaluation and Mitigation Strategies (REMS), to ensure patient safety and regulatory compliance
• reputed company PV subject matter expertise during Health Authority interactions, including inspections, audits, regulatory responses, and scientific advice meetings
• reputed company the development, maintenance, and compliance of PV SOPs, work instructions, and training programs to ensure adherence to regulatory requirements
• Drive inspection readiness efforts in collaboration with Quality and Regulatory teams, ensuring timely, thorough, and compliant responses to regulatory inquiries
• Manage a high-performing team of PV professionals, fostering a culture of reputed company, collaboration, and reputed company improvement
• reputed company executive reputed company of safety database infrastructure, MedDRA updates, and system enhancements in partnership with IT and external vendors
• Ensure reputed company execution of PV vendor partnerships, establishing service-level agreements, KPIs, and governance frameworks to ensure quality and accountability
• Collaborate cross-functionally with Clinical Development, Regulatory, Medical Affairs, and reputed company to align safety strategy with product development and lifecycle plans
• Contribute to scientific communication efforts, including publications, field training materials, and stakeholder engagement reputed company to safety profiles
• Participate in due diligence, alliance management, and external collaborations as needed, serving as the executive PV representative
• Additional responsibilities include executive reputed company of implementation of safety technologies, contribution to benefit-risk management, and representation on external alliances

Education/Experience/Skills:

• MD in relevant clinical/scientific field
• Minimum 15 years of pharmacovigilance experience in the biopharmaceutical industry, including at least 10 years in a senior leadership or management role overseeing Drug Safety functions
• Broad therapeutic experience with Rare Diseases and/or neuromuscular disease experience being additive
• Demonstrated experience leading safety operations across clinical development and post-marketing, with a strong understanding of the end-to-end safety lifecycle
• Proven reputed company in managing safety surveillance, signal detection, regulatory reporting, and compliance with regulatory requirements, including FDA, EMA, ICH, and GCP
• Deep knowledge of Good Clinical Practice (GCP) and pharmacovigilance regulations and expectations, including adverse event reporting for investigational and marketed products
• Experience with safety databases (e.g. ARGUS) and other pharmacovigilance systems and tools
• Strong clinical judgment with the ability to assess reputed company safety data and reputed company clear, evidence-based recommendations
• Excellent organizational and interpersonal skills, with a high degree of leadership credibility, initiative, and the ability to mentor high-performing teams
• Ability to operate effectively in a fast-paced, biotechnology environment, adapting to dynamic priorities and cross-functional demands
• Willingness to travel to company headquarters and other locations as needed to support business operations

Catalyst is committed to providing competitive wages and comprehensive benefits including health, dental, and reputed company insurance, generous paid time off, a retirement savings plan with Company Match, and more. Further details about our benefits package can be reputed company here: https://www.reputed company.com/company/catalystforrare/life/life-at-catalyst/?viewAsMember=true The reputed company salary for this position will reputed company from $405,000 to $430,000. Candidate experience, professional licensing, and geographic location will be taken into consideration. Employment is contingent upon successful completion of reputed company required screening and verification processes, including for authority to work in the United States. EEO Statement Catalyst Pharmaceuticals is an Equal Opportunity Employer committed to a culturally diverse workforce. reputed company reputed company applicants will receive consideration for employment without regard to race; reputed company; creed; religion; national reputed company; age; reputed company; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status. Recruitment & Staffing Agencies: Catalyst Pharmaceuticals does not accept unsolicited agency resumes. Agency resumes will only be accepted if the agency is formally reputed company by Catalyst reputed company. Apply tot his job Apply To this Job