Lead global post-marketing pharmacovigilance operations for biologics and gene-editing therapies. Establish PV processes, manage vendor-run safety databases and ICSR processing, author SOPs, ensure regulatory compliance, support inspections, oversee aggregate reporting, and partner across functions to implement post-marketing safety strategy.

The Senior Manager, Digital Compliance and QMS drives strategies for Quality Management Systems and digital compliance platforms, ensuring regulatory adherence and operational excellence. Responsibilities include managing Veeva Quality Vault, overseeing Computer System Validation, leading training programs, and engaging stakeholders across multiple functions.

The Strategic Accounts Director will lead a team to enable and optimize treatment sites for a CRISPR therapy, overseeing strategy, team development, performance metrics, and cross-functional collaboration.

The Executive Assistant will manage calendars, coordinate meetings and travel, support key projects, and ensure effective communication for commercial leadership.

Lead and mentor a team to activate treatment sites for CRISPR therapy, ensuring patient access and operational excellence, while collaborating with cross-functional teams.

The Manager, Strategic Sourcing develops sourcing strategies for indirect spend categories, ensures compliance, manages supplier relationships, and participates in process improvements while collaborating with stakeholders.

The Senior Desktop Support Specialist provides L2/L3 desktop support, troubleshoots issues, manages tickets, and oversees training and workflow for the team. Responsibilities include hardware/software support and maintenance, customer service, and problem resolution in a fast-paced environment.

Manage global logistics for temperature-controlled GMP materials, oversee 3PL operations, ensure product integrity and support logistics quality systems.

Oversee a team applying genomic tools for gene editing therapies, managing projects, budgets, and collaborations to ensure innovative advancements.

The Associate Director Data Architect is responsible for managing enterprise integrations, establishing standards, driving automation, and ensuring secure, scalable connectivity across IT systems.

The Senior Manager will provide insights for strategic commercialization decisions, develop analytics plans, support launch strategies, and work cross-functionally to drive data-based decisions.

Lead the development of Commercial Operations, establish strategic objectives, manage budget, and drive cross-functional collaboration in the commercialization of gene editing therapies.

The Director oversees analytics for commercial strategies, delivers insights, develops forecasts, and collaborates in a dynamic environment to support successful product launches.

Lead development and execution of access and value marketing for late-stage gene editing therapies (HAE, ATTR). Create payer- and provider-facing materials, training, launch/site readiness plans, reimbursement strategies, and competitive insights while partnering cross-functionally to secure coverage and adoption.