Associate Clinical Development Director
2 days ago
Job Description:
About the Associate/Clinical Development Medical Director (CDMD)The CDMD is responsible for leading the planning and management of assigned RLI clinical programs to support RTL trials from an end-to-end clinical development perspective.
As CDMD, you will have oversight of assigned programs and drive execution of the plan, enabling an empowered organization that can navigate a matrix environment and adjust quickly to business needs.
You will provide clinical leadership and strategic medical input for all clinical results in assigned projects, leading the development of clinical sections of trial and program level regulatory documents.
You will also drive execution of programs and clinical trials, supporting 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.
Key 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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