Global Product Development Lead – Late-Stage Therapeutics
Location: United States (Preferred) / United Kingdom / Switzerland – Permanent Position (Remote)
About the Role
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.
Key Responsibilities
- Lead and oversee international, cross-functional asset teams through late-stage development programs, particularly Phase III clinical trials.
- Develop and execute product development strategies within pharmaceutical or biotechnology settings, managing complex molecules such as biologics.
- Drive development programs across multiple functional areas, including clinical, regulatory, CMC, and strategic planning, ensuring alignment with global stakeholders.
- Balance strategic oversight with hands-on execution when necessary to meet program milestones.
- Manage stakeholder communication and influence senior leadership across regions, ensuring smooth project progression.
- Navigate product lifecycle development from late-stage, through submission, to approval pathways.
- Strongly contribute to non-clinical development activities and provide input on regulatory and CMC strategies.
Requirements
- Minimum 5+ years of experience as a global product development lead, with proven success in late-stage development programs.
- Experience with phase III late-stage development.
- Strong CMC and regulatory expertise, especially for late-stage programs.
- Significant experience in leading international, cross-functional teams on complex development initiatives.
- Expertise in product development strategy within pharmaceutical or biotech environments, particularly with biologics or complex molecules.
- Demonstrated ability to manage and align multiple global stakeholders and execute at senior leadership levels.
- Deep understanding of product lifecycle development, including regulatory and submission pathways.
- Excellent communication and leadership skills, with the ability to influence senior stakeholders across regions.
- Experience operating within highly matrixed, international organizations.
- Fluency in English, both written and spoken.
Preferred Qualifications
- Experience within oncology programs is advantageous but not required.
- Exposure to radiopharmaceuticals or next-generation therapeutics is a plus.
- Experience in non-clinical development activities.
- Commercial awareness or understanding of market access considerations.
- Proven leadership of global programs in US-based organizations and adaptability across therapeutic areas and modalities.
- A pragmatic leadership style with a focus on implementation and execution.
- Interest in joining a fast-evolving, innovative therapeutic platform at a senior strategic level.
Sound interesting?
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or send me a message!