Clinical Program Head

We are seeking for a US- based Clinical Program Head who will lead the strategic, scientific, and operational direction of assigned clinical development programs. The role involves working closely with global stakeholders and experts, and driving delivery of high-quality clinical programs within scope, time, and budget.

Key Responsibilities:

Lead clinical program strategy and provide scientific leadership across assigned programs
Own delivery of clinical program milestones and outputs, ensuring quality, timelines, and budget adherence
Oversee the development and finalization of key clinical documents including study protocols, investigator brochures, regulatory submissions, and publications
Maintain oversight of patient safety activities including signal detection and ongoing surveillance
Provide cross-functional leadership in collaboration with clinical operations, finance, regulatory, and other functions
Engage with regulatory agencies, KOLs, investigators, and advocacy groups as a trusted scientific leader
Identify and manage risks; develop mitigation and contingency strategies
Contribute to R&D portfolio strategy and organizational alignment

Experience & Qualifications:

Medical Degree (MD) required
Minimum of 6 years’ experience in clinical drug development, with a strong track record in trial design, execution, and regulatory submission
Proven leadership capabilities, including people and matrix management
Disease area expertise (preferably oncology or nuclear medicine)

Key Competencies:

Strong scientific and clinical acumen with excellent communication skills
Strategic mindset with influencing and negotiation skills
In-depth understanding of GCP, clinical trial design, and the drug development lifecycle
Familiarity with nuclear medicine/oncology-specific clinical development is desirable
Willingness to travel internationally (approx. 20%)
Fluent in English (written and spoken)