Clinical Development Medical Director Lead
4 days ago
About the Role
- As a key member of our team, you will provide clinical leadership and strategic medical input for all clinical results in assigned projects.
- You will lead the development of clinical sections of trial and program level regulatory documents, ensuring compliance with relevant regulations.
- In partnership with global line functions, you will drive execution of programs and clinical trials, achieving timely and successful outcomes.
- You will support the overall safety of molecules by ensuring adherence to safety protocols and collaborating with Patient Safety colleagues.
- As a nuclear medicine physician specialist, you will contribute to interactions with external and internal partners, providing medical expertise and guidance.
- You will contribute to the publication strategy of compounds from a scientific standpoint, leveraging your expertise to inform stakeholders.
- Your work may involve collaboration with Biomedical Research/Translational Medical Sciences to drive transition of pre-PoC projects to DDP and with Business Development & Licensing, including target identification and due diligence.
Role Requirements:
- Nuclear medicine Physician/Medical Doctor with a sophisticated knowledge and clinical training in oncology PET.
- At least 5 years of clinical practice experience is preferred.
- Experience in Clinical Trials with a PET component is essential.
- Experience with Radioligand therapy is also required.
- You must be able to interpret, discuss, and present data relating to clinical trial(s) with a Nuclear Medicine component.
- A proven ability to establish effective scientific partnerships with key partners is essential.
- You should have a solid understanding of GCP, clinical trial design, statistics, regulatory, and clinical development processes.
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