Note The job is a remote job and is open to candidates in USA. Kura Oncology is a clinical-stage biopharmaceutical company focused on precision medicines for cancer treatment. They are seeking an reputed company Associate Director/Director of Pharmacovigilance Operations to reputed company their global pharmacovigilance infrastructure, overseeing outsourced safety operations and ensuring compliance with regulatory requirements.

Responsibilities

• reputed company the process for ICSR collection, processing, reconciliation, and reporting, including associated quality activities to ensure regulatory timelines and global standards are met.
• Provide reputed company and support of the PV vendor activities, including establishing and monitoring key performance indicators (KPIs), always ensuring inspection-readiness.
• reputed company global compliance with pharmacovigilance regulations, including timely ICSR submissions, quality 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 clinical databases, as well 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 Action (CAPA) activities reputed company to, but not limited to, expedited and periodic reporting activities, as well as deviations reputed company to case management processes, as defined in the SMPs or SOPs.
• Collaborate with Clinical Operations to deliver 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, Clinical Operations, Clinical Development, Data Management, Quality 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.
• Provide PV operational expertise in development of RMPs, REMS, DSURs, PSURs, and other safety deliverables.
• Represent PV operations in internal safety governance forums and external 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 field 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 Operations.
• 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 pre- and post-marketing Safety, with proven success in biotech or small/mid-sized pharma, ideally in a lean team setting.
• Experience supporting late-stage clinical 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, Arisglobal, Vault Safety) required.
• Able to work independently, establish work priorities, and execute decisions with minimal 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 strategic, decision-making and analytical skills.
• Excellent collaboration and strong written and verbal communication skills are required.
• Experience working with clinical 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 options
• ESPP Plan
• 20 days of PTO to start
• 18 Holidays (Including Summer & Winter Break)
• Generous Benefits Package with a variety of plans available with a substantial employer match
• Paid Paternity/Maternity Leave
• In-Office Catered lunches
• Home Office Setup
• Lifestyle Spending Stipend
• Commuter Stipend (Boston Office)
• Regula