【AstraZeneca】【R&D】Project Physician,Baselga Cancer Research Scholar

Location
Japan - Osaka
Workplace
On-site

About this role

Typical Accountabilities
- Review scientific literature and consult with internal experts to identify biological mechanisms underlying pathophysiology and potential drug effects.
- Assist in designing and executing studies by preparing pharmacogenetics components of clinical study protocols to assess biological mechanisms.
- Liaise with Clinical Pharmacology colleagues to assist in designing and executing Phase I to Phase III Clinical Trials to establish Proof of Principle and support Proof of Concept.
- Initiate and monitor epidemiological research conducted by external scientific groups while providing medical expertise to non-physician epidemiology colleagues.
- Act as a regional technical expert, delivering strategic input, offering consultancy, and supporting the Physician area of specialization.
- Evaluate safety and pharmacodynamic aspects of early-stage clinical trials for new compounds.
- Deliver pharmacogenetics contributions to Translational Science Plans and Clinical Development Plans to enhance research outcomes.
- Supervise volunteers in medical trials and review safety assessments to ensure compliance with protocols.
- Lead development of statistical standards or techniques to improve project quality, efficiency, and overall Group effectiveness.
- Conduct specialized research to enhance Biostatistics contributions to global product submissions across a range of therapies.
- Provide strategic input, statistical expertise, and leadership in designing and interpreting clinical studies and study programs.
- Apply medical expertise to support internal proposal development and external regulatory submissions effectively.
- Serve as a knowledge source in areas of expertise, defining and communicating key initiatives across various departments and functions.
- Establish and implement policies, procedures, and objectives in work or team areas to ensure compliance with internal and external regulations.
- Offer professional expertise to design, analyze, and interpret epidemiological studies while performing in-depth epidemiological literature reviews.
- Promote good physician practices and ensure adherence to relevant protocols in clinical trials.
- Develop operational systems and refine research processes across responsibilities to improve project efficiency and effectiveness.

Qualifications and Skills
Essential: Medical degree; Thorough knowledge of study analysis and design in all phases of drug development; Experience of modelling and simulation to improve execution of studies.
Desirable: Extensive general medical knowledge.

Key Relationship to Reach Solutions
Internal: Members of all functions on project team; Members of Development.
External: External service providers; External regulatory agencies.

Date Posted

16-9月-2026

Closing Date

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Tired of cold applications?

Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.

Know someone who'd be great for this?