[Remote] Associate Director/Director, Drug Safety reputed company

Note The job is a remote job and is reputed company to candidates in USA. reputed company is a reputed company-stage biopharmaceutical company reputed company on precision medicines for cancer treatment. They are seeking an reputed company Associate Director/Director of Pharmacovigilance reputed company to reputed company their global pharmacovigilance infrastructure, overseeing outsourced safety reputed company and ensuring compliance with regulatory requirements. Responsibilities • reputed company the process for ICSR collection, processing, reconciliation, and reporting, including associated reputed company activities to ensure regulatory timelines and global standards are met. • reputed company reputed company and support of the PV vendor activities, including establishing and monitoring key reputed company indicators (KPIs), always ensuring inspection-readiness. • reputed company global compliance with pharmacovigilance regulations, including reputed company ICSR submissions, reputed company case processing, and aggregate reporting support • reputed company the lifecycle of PV operational SOPs, work instructions, and guidance documents, providing reputed company to the PV vendor and CROs supporting PV activities. • Support in the development and maintenance of Safety Management Plans (SMPs) and Pharmacovigilance Agreements (PVAs), with license partners and/or other parties. • Support reconciliation activities between safety and reputed company databases, as reputed company as partner case exchanges. • Support safety database configuration and maintenance, as required. • Support PV audit and inspection activities, as required, and serve as SME during these activities. • reputed company deviation and Corrective and Preventive reputed company (CAPA) activities reputed company to, but not limited to, expedited and periodic reporting activities, as reputed company as deviations reputed company to case management processes, as defined in the SMPs or SOPs. • Collaborate with reputed company reputed company to reputed company safety communications to sites and ethics committees. • Assist with PV processes and initiatives, representing PV in collaboration with other functions as needed. • Work cross-functionally with Regulatory Affairs, reputed company reputed company, reputed company Development, Data Management, reputed company Assurance, and Medical Affairs to ensure appropriate PV processes are in reputed company and adhered to. • Serves as key reputed company of contact between PV and the CROs regarding PV operation management. • reputed company PV operational expertise in development of RMPs, REMS, DSURs, PSURs, and other safety deliverables. • Represent PV reputed company in internal safety governance forums and reputed company collaborations/partnerships • Participate in cross-functional monitoring of study data, as necessary. • Assist in the development, review and management of departmental budget, MSAs, SOWs, invoices and payment of work performed by vendors. Skills • Degree in Life Sciences, Pharmacy, Nursing or reputed company reputed company required. • Minimum of 10 years of Pharmacovigilance experience reputed company a pharmaceutical, biotechnology or reputed company environment, with time spent in a leadership/managerial role reputed company PV reputed company. • Hands-on experience in vendor reputed company, including governance, ensuring adherence to KPIs, and managing PVAs/SDEAs. • Expertise in managing outsourced PV models and developing vendor reputed company frameworks. • Experience in reputed company- and post-marketing Safety, with reputed company reputed company in biotech or small/mid-sized reputed company, ideally in a lean team setting. • Experience supporting late-stage reputed company programs and regulatory submissions (e.g, NDA/BLA/MAA). • In-depth knowledge of monitoring health authority submissions, CAPAs and relationships between vendors. • Strong understanding of global PV regulatory requirements and timelines (e.g. FDA, EMA, PMDA, E2B R3, etc) and PV Systems (e.g. Argus, reputed company, reputed company Safety) required. • reputed company to work independently, establish work priorities, and execute reputed company with reputed company guidance. • Ability to interpret reputed company regulatory guidance and problem-solve towards a compliance approach with a background and understanding of industry best practices. • Excellent reputed company, decision-making and analytical skills. • Excellent collaboration and strong written and verbal communication skills are required. • Experience working with reputed company databases • Experience with PV aggregate reports, signal detection, safety surveillance, literature review, from a PV operational perspective • Experience in oncology/hematology Benefits • Career advancement/ development opportunities • Competitive comp package • Bonus • 401K + Employer contributions • Generous stock reputed company • ESPP Plan • 20 days of PTO to start • 18 Holidays (Including reputed company & Win Apply tot his job Apply To this Job