PI
Posted 1 day ago
Global Product Development Lead
Panda International
📍 London
ScientificRemoteFull-time
Job description
<p><strong>Global Product Development Lead – Late-Stage Therapeutics</strong></p><p>Location: United States (Preferred) / United Kingdom / Switzerland – Permanent Position (Remote)</p><p><br><br>Check all associated application documentation thoroughly before clicking on the apply button at the bottom of this description.<br></p><p><strong>About the Role</strong></p><p>We are seeking a highly experienced Global Product Development Lead to join our team in a senior management capacity. This role is focused on late-stage therapeutic development within the radiopharma sector and offers a remote work environment with a preference for candidates based in the United States, United Kingdom, or Switzerland. The position is full-time and permanent.</p><p><br></p><p><strong>Key Responsibilities</strong></p><ul><li>Lead and oversee international, cross-functional asset teams through late-stage development programs, particularly Phase III clinical trials.</li><li>Develop and execute product development strategies within pharmaceutical or biotechnology settings, managing complex molecules such as biologics.</li><li>Drive development programs across multiple functional areas, including clinical, regulatory, CMC, and strategic planning, ensuring alignment with global stakeholders.</li><li>Balance strategic oversight with hands-on execution when necessary to meet program milestones.</li><li>Manage stakeholder communication and influence senior leadership across regions, ensuring smooth project progression.</li><li>Navigate product lifecycle development from late-stage, through submission, to approval pathways.</li><li>Strongly contribute to non-clinical development activities and provide input on regulatory and CMC strategies.</li></ul><p><br></p><p><strong>Requirements</strong></p><ul><li>Minimum 5+ years of experience as a global product development lead, with proven success in late-stage development programs.</li><li>Experience with phase III late-stage development.</li><li>Strong CMC and regulatory expertise, especially for late-stage programs.</li><li>Significant experience in leading international, cross-functional teams on complex development initiatives.</li><li>Expertise in product development strategy within pharmaceutical or biotech environments, particularly with biologics or complex molecules.</li><li>Demonstrated ability to manage and align multiple global stakeholders and execute at senior leadership levels.</li><li>Deep understanding of product lifecycle development, including regulatory and submission pathways.</li><li>Excellent communication and leadership skills, with the ability to influence senior stakeholders across regions.</li><li>Experience operating within highly matrixed, international organizations.</li><li>Fluency in English, both written and spoken.</li></ul><p><br></p><p><strong>Preferred Qualifications</strong></p><ul><li>Experience within oncology programs is advantageous but not required.</li><li>Exposure to radiopharmaceuticals or next-generation therapeutics is a plus.</li><li>Experience in non-clinical development activities.</li><li>Commercial awareness or understanding of market access considerations.</li><li>Proven leadership of global programs in US-based organizations and adaptability across therapeutic areas and modalities.</li><li>A pragmatic leadership style with a focus on implementation and execution.</li><li>Interest in joining a fast-evolving, innovative therapeutic platform at a senior strategic level.</li></ul><p><br></p><p>Sound interesting? xwzovoh </p><p>Send your CV to Khanyi Mabena at or send me a message!</p>