<p>Our Opportunity…</p> <p>We are looking for a proactive and detail-oriented Associate Director of Program Management to join our dynamic team.</p> <p>The ideal candidate will be responsible for driving exceptional cross-functional project execution, ensuring transparency and alignment across CMC, clinical, regulatory, quality, and research, functions to achieve our ambitious goals. This individual will play a key role in supporting project planning, tracking milestones, mitigating risks, and facilitating decision-making to advance the company's programs efficiently and effectively.</p> <p>This is a unique opportunity to contribute to advancing a novel cell therapy that has the potential to become a meaningful option for patients with advanced or metastatic melanoma and other solid tumors. Supported by blue chip investors, field-leading advisors, best-in-class partners, and an experienced team, you'll be part of a dynamic, innovative, passionate, and collaborative team.</p> <p>You Will…</p> <ul> <li>Lead project planning, execution, and monitoring activities across cross-functional teams, ensuring deliverables are met on time and within scope. </li><li>Develop and maintain detailed project plans, timelines, dashboards, decision trackers, risk registers, and communication tools to support program transparency and accountability. </li><li>Facilitate regular project team meetings, drive agenda setting, capture action items, and ensure timely follow-up. </li><li>Identify and manage project risks and issues; propose mitigation strategies and escalate as appropriate. </li><li>Partner closely with CMC, Clinical, Regulatory, Quality, and R&D teams to ensure seamless coordination of activities. </li><li>Support governance presentations and status updates for internal leadership and external stakeholders. </li><li>Assist with budget tracking, resource forecasting, and vendor management in collaboration with functional leads. </li><li>Contribute to continuous improvement of project management processes, tools, and templates. </li><li>Foster a culture of accountability, collaboration, and proactive problem-solving across all teams. </li></ul> <p>You Bring…</p> <p>Core Qualifications</p> <ul> <li>Bachelor's degree in Life Sciences, Engineering, or a related field with 10+ years of experience; advanced degree (M.S./Ph.D. 8+) or PMP certification is a plus. </li><li>5+ years of experience in biotechnology, pharmaceuticals, or life sciences program management; cell therapy or other oncology experience highly preferred. </li><li>Strong understanding of drug development process including Clinical, Regulatory, and/or CMC, especially pivotal-to-BLA </li><li>Proven ability to manage complex, cross-functional projects to meet aggressive goals in a fast-paced, dynamic environment. </li><li>Successful experience interfacing with external partners (CDMOs, CROs etc.) </li><li>Proficiency with project management tools (e.g., MS Project, Smartsheet, or equivalent). </li><li>Demonstrated experience in developing timelines, risk assessments, and budget tracking. </li><li>Highly collaborative mindset with the ability to lead without direct authority. </li></ul>