The Associate Director, PV Scientist oversees pharmacovigilance data, ensuring regulatory compliance, enhancing safety infrastructure, conducting signal detection, and managing safety narratives and reports.

Manage, file, and quality-check essential clinical trial documents in the eTMF. Track and resolve quality issues, support filing/archiving across studies, and improve filing processes alongside TMF leadership.

Lead analytical development activities for drug products and substances, ensuring compliance with GMP standards and overseeing external providers. Collaborate with CMC teams to optimize processes and deliver product quality.

The Director of Investor Relations will develop the company's investor relations strategy, articulate investment theses, prepare earnings materials, and manage investor communications, ensuring compliance and value creation.

The Monitoring Oversight Lead will oversee monitoring operations, ensure quality data management, perform risk assessments, and prepare monitoring reports while training staff and ensuring compliance.

The Director of Commercial Compliance will develop and lead the compliance program for product launches, ensuring regulatory adherence and operational support across various departments while providing training and risk assessments.

The Director of Commercial FP&A leads financial planning and analysis for a commercial organization, focusing on launch readiness, revenue forecasting, and strategic finance partnerships with cross-functional teams.

Manage Microsoft Intune configurations, device compliance, and support for a remote workforce, ensuring security across endpoints.

The Senior Accountant will support monthly close, prepare financial reports, and assist with FP&A functions related to budgeting and forecasting.

The Associate Director will lead quality oversight for commercial and clinical supply chains, ensuring GMP compliance, and driving operational excellence across cross-functional partnerships.

The Quality Operations Manager oversees quality assurance activities, manages regulatory compliance, coordinates with contract service providers, and leads product quality and operational initiatives throughout the product lifecycle.

The Senior Director leads global pharmacovigilance operations, ensuring compliance, managing safety reporting, and collaborating across functions while overseeing vendor relationships and enhancing capabilities.

Lead sales strategy and execution for Praxis, building and managing high-performing teams, establishing sales targets, and collaborating with cross-functional teams to drive growth in the biotech/pharmaceutical sector.

Lead oversight of data management for assigned studies, manage external vendors, review and approve DM documentation, perform secondary UAT of EDC, implement RBQM oversight, and provide cross-functional input on protocols and study deliverables to ensure data quality and regulatory compliance.

Manage analytical development projects, ensure compliance with GMP standards, oversee external partners, and support CMC stability programs in drug development.