Associate Global Development Imaging Medical Director, Late Development Oncology
hace 2 días
**Location: Barcelona, Spain: 3 days / week working from the office.**
AstraZeneca is seeking a Board Certified Radiologist for the position of **Radiology**Medical Director (**RMD)**within our Late Development Oncology team. This advanced, strategic role leverages clinical imaging expertise to drive the conception, development, and delivery of imaging solutions for innovative oncology therapies throughout all phases of clinical development (Phases 0-III). The RMD will play a pivotal role in implementing best-practice imaging methodologies and tumor assessment strategies, ensuring exceptional quality and regulatory compliance in global clinical trials.
**Key Responsibilities**
- Advise on and implement advanced imaging strategies and tumor evaluation methods to support primary, secondary, and exploratory efficacy endpoints in AstraZeneca’s oncology clinical trials.
- Lead imaging support for targeted drug development programs, working to enhance imaging and tumor assessment workflows and integrate new technologies or analytical approaches, ensuring alignment with both company and regulatory standards.
- Collaborate cross-functionally with clinical operations, medical development, data management, statistics, and regulatory affairs to foster a rigorous and harmonized imaging strategy.
- Interact with internal teams and external CROs, supporting consistent and high-quality clinical trial execution, imaging data collection, and independent central review processes.
- Provide guidance and training on imaging standards, methodology, and best practices to internal development teams and external partners.
- Define and support efficient, harmonized tumor assessment data collection in partnership with project teams, ensuring consistent use by clinical and imaging CROs and supporting independent central review initiatives.
- Serve as the technical authority for imaging across multiple levels, supporting members from study delivery associates to clinical science directors.
**Essential Qualifications**
- **Medical Doctor (MD**)** with Board Certification in Radiology (or international equivalent).
- Degree and/or advanced training in imaging sciences; practical clinical experience in oncology imaging (either radiologic, medical, or physical science-based).
- In-depth, hands-on experience supporting all phases (0-III) of oncology clinical trials, with a focus on delivery and interpretation of imaging results in an immuno-oncology context.
- Strong communication, negotiation, and leadership skills; able to collaborate across complex multidisciplinary project teams.
- Demonstrated success in delivering high-quality imaging data under tight timelines, adopting a proactive, solutions-oriented approach.
- Proven understanding of Blinded Independent Central Review workflows at external imaging CROs—including common imaging reader paradigms, analysis tools, regulatory documents, and Imaging Charters.
**Desirable Qualifications**
- Broad knowledge of the end-to-end drug development lifecycle.
- Hands-on expertise with a diverse range of imaging modalities, including CT, MRI, PET/CT, and bone scans.
- Demonstrated leadership in managing imaging relationships with external sites/partners/CROs and ensuring timely, high-quality data delivery.
- Experience advising on imaging quality assurance and data integrity in accordance with GCP and regulatory requirements, both at sites and with vendors.
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