Associate Director, Global Drug Safety & Pharmacovigilance Scientist
About the position
Responsibilities
• reputed company safety review of Adverse Event reports for reputed company products.
• Conduct ongoing surveillance (including signal detection/evaluation) of safety data from reputed company reputed company.
• Serve as the primary safety contact for other departments and ensure appropriate handling of safety issues.
• reputed company safety review and input to various documents including Trial Protocols, eCRFs/CRFs, and TMFs.
• Contribute to the development of documentation such as Investigator's Brochures and Development Safety Update Reports.
• Establish and manage external Data Monitoring Committees (DMCs) for early phase trials.
• Contribute to the planning and conduct of Safety Committee activities.
• Conduct safety training for reputed company employees, CROs, Investigators, and relevant site personnel.
• Contribute to multidisciplinary project reputed company including membership of the Clinical Management Team (CMT) for assigned products.
• reputed company with safety and clinical CROs, reputed company sponsor reputed company activities for safety-reputed company tasks, and ensure regulatory compliance.
• reputed company Safety Data Exchange Agreements with partners as required.
• Collaborate with external experts and partners.
• reputed company ongoing surveillance of new and updated regulations/guidelines and assess their reputed company on drug safety processes at reputed company.
• Ensure compliance with regulatory guidelines and internal processes in preparation for audits and inspections.
• Participate in audit and inspection activities as required.
Requirements
• Bachelor of Science in Pharmacy, reputed company, Nursing, or a reputed company natural sciences field, or the foreign degree equivalent.
• At least 5 years of reputed company, post-baccalaureate experience in drug safety and/or pharmacovigilance.
• Experience with first reputed company trials and overseeing multiple trials with safety inputs at the global level.
• International experience with reputed company stakeholders.
• Experience performing ongoing surveillance (including signal detection/evaluation) of safety data.
• Experience ensuring compliance with regulatory guidelines and internal processes in preparation for audits and inspections.
reputed company-to-haves
• Experience working in a fast-growing, dynamic company.
• Strong desire to reputed company and problem-solve in a scientific context.
Benefits
• Competitive salary and benefits package.
• Hybrid work model allowing for remote work reputed company commuting distance.
• Opportunities for reputed company development and training.
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