Join Our Crew

Responsibilities Include

• Work with the CMR portfolio PM and lead Asset PM to align program planning and execution with corporate objectives and Product Development Team (PDT) strategy.
• Develop project scope, timelines, budgets, and resource plans across the clinical portfolio.
• Lead cross-functional study team and governance meetings, including agendas, decision logs, minutes, action-item tracking, collaboration, and team alignment.
• Partner with Clinical Operations, Clinical Development, Biometrics, Medical Affairs, and Regulatory leaders to develop and maintain project plans, timelines, and dashboards for multiple clinical programs aligned with department and corporate objectives.
• Identify, score, and communicate risks through maintained risk registers with proactive mitigation and contingency plans; ensure department timelines and risk trackers integrate with the corporate portfolio and integrated roadmaps.
• Manage CROs, vendors, and external partners by tracking performance and contracts, escalating and resolving issues, leading vendor governance meetings, and cultivating durable relationships focused on on-time, quality delivery.
• Support preparation and submission of regulatory filings, including INDs and BLAs, in partnership with Clinical, Regulatory Affairs, Technical Development, and Supply Chain.
• Prepare and present project updates to senior management and key stakeholders to support decision-making; partner with Finance and Legal to facilitate on-time, on-budget milestone delivery.
• Advance enterprise PMO best practices by creating and using PM tools and templates that support continuous improvement and scalable processes.
• Serve as Smartsheet Super User by building and publishing project and portfolio-level plans, dashboards, and reports, and training team members on Smartsheet functionality.
• Work across time zones as necessary; travel 10–15% may be required; other duties as assigned.

Required Qualifications

• Experience in pharmaceutical or biotechnology industries is required.
• 7+ years of program management experience is required for Sr. Manager level; 8+ years is required for Associate Director level. Technical operations experience and cell and gene therapy, CAR-T, or similar industry experience are preferred.
• Direct experience supporting regulatory Health Authority Inspections in a GxP-regulated environment is required.
• Proficiency in MS Office, including Outlook, PowerPoint, Excel, and Word, and familiarity with project management tools are required.
• Strong understanding of PM best practices, PMO operating models, and scalable processes in a growing corporate environment is required.
• Extensive Smartsheet experience, including creating, maintaining, and reporting timelines, Gantt charts, dashboards, and reports.
• Excellent external-facing presence and experience managing vendor relationships and contracts.
• Strong verbal and written communication skills.
• Outstanding attention to detail with the ability to manage multiple tasks and priorities.
• Ability to work both independently and collaboratively with cross-functional teams.
• Thrives in a dynamic, fast-paced, timeline-based environment.
• Strong customer service focus as part of PM culture.

Preferred Qualifications:

• Advanced degree in Life Sciences is preferred.
• Certification in project management, such as PMP or CAPM, is preferred.
• Experience with both early- and late-stage clinical programs is an advantage.
• Cell and gene therapy, CAR-T, or similar industry experience is preferred.

Apply For This Job