Expression of Interest: Medical Directors (MD)
- Clinical Leadership: Provide strategic medical input and leadership for all clinical deliverables within assigned projects or clinical programs.
- Regulatory Documentation: Lead the development of clinical sections for trial and program-level regulatory documents (e.g., protocols, investigator brochures, clinical study reports).
- Program Execution: Drive the execution of clinical trials in collaboration with global line functions, Global Trial Directors, and regional/country medical associates.
- Safety Oversight: Support the Global Program Clinical Head (GPCH) in ensuring the safety of the molecule, including participation in the Safety Management Team and collaboration with Patient Safety colleagues.
- Strategic Planning: Contribute to the Clinical Development Plan (CDP), Integrated Development Plan (IDP), and disease area clinical standards.
- Cross-functional Collaboration: Act as a medical expert in interactions with internal stakeholders (e.g., Translational Medicine, Business Development & Licensing) and external partners.
- Innovation & Transition: Support the transition of pre-proof-of-concept (PoC) projects to full development and contribute to target identification and due diligence processes.
- Education: MD or equivalent medical degree required.
- Experience:
- Clinical research or drug development.
- Clinical practice experience (4+ years including residency) preferred.
- We are looking for physicians with specialization and deep expertise in our core therapeutic areas including Radioligand therapy (RLT), Immunology, Rheumatology, Dermatology, Nephrology, Oncology, T-Charge (CAR-T).
- Skills:
- Strong understanding of GCP, clinical trial design, and regulatory processes.
- Proven ability to interpret and present clinical data.
- Effective communicator with experience in matrixed, global environments.
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