Baselga Cancer Research Scholar

AstraZeneca•Waltham, MA

22h

About The Position

The Baselga Cancer Research Scholars Program, now in its sixth year, is a 2-year immersive education and research program for early-career Oncologists who are inspired by science and by how clinical development has the potential to transform patient care. As part of a competitively selected cohort of Scholars, you will be based in Oncology R&D with an opportunity to learn from a diverse group of experts across the drug development continuum, playing a pivotal role in channelling our scientific capabilities to make a positive impact on changing patients’ lives. Selected Scholars will join the current cohort of Baselga Cancer Research Scholars, to build a strong community of drug developers. We are currently recruiting for the 2026 class with an aim to start the position in summer-autumn 2026. About AstraZeneca Oncology Research & Development Our Oncology strategy is built with one goal in mind – pushing the boundaries of science to deliver life-changing medicines to patients. We have a passion for discovery and a broad pipeline of next-generation medicines, and together with a focus on execution excellence, we aim to expand treatment options and improve outcomes for patients with solid and haematological cancers. We’re pioneering innovative research across six scientific platforms: Tumor drivers and resistance; Immuno-oncology, DNA damage response, Antibody drug conjugates, Epigenetics and Cell therapies. Our ambition is to eliminate cancer as a cause of death. It’s our big vision that unites and inspires us. With multiple indications and high-quality molecules at all stages of our innovative pipeline, we keep pushing forward. Focusing on cutting-edge science with the latest technology to achieve breakthroughs. AZ is a place built on courage, curiosity and collaboration – we make bold decisions driven by patient outcomes. The 2026 AZ Baselga Cancer Research Scholars cohort will join AstraZeneca at a time of tremendous growth and acceleration in the oncology biologics portfolio. Working in a fast-paced and dynamic work environment you will experience increasing levels of responsibility, following a structured learning plan in the following domains: 1) Clinical Study Assignment: You will join a clinical study team and build experience as a medical leader in clinical development which could be in Early Clinical Development, Late Clinical Development, or one year in each. You will participate in weekly clinical and scientific meetings related to your clinical study, complete AstraZeneca training programs and participate in internal and external scientific meetings. You will work in a cross functional environment, . contributing to and supporting Department/Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional/organization processes designed to effectively deliver our R&D portfolio. 2) Rotational program: During the course of your program, you will be involved in 3-6 month long rotations across various groups to gain a better understanding of the cross-functional departments. This could include: Patient safety, Clinical operations, Regulatory affairs, Biostatistics, Medical affairs, Translational medicine or precision medicine 3) Longitudinal Research Project: You will have opportunity to undertake a research project for the duration of the 2-year program, which may be an area of specialist interest to you and AstraZeneca, or alternatively focus on one or more of the rotational functions. The intent is that this will be presented at the end of the Program to key internal stakeholders, as well as at a key scientific meeting and published in a peer-reviewed journal.

Requirements

MD/Physician required; ideally board certified in Oncology or Haematology/Oncology
2 - 3 years of clinical oncology training required
Excellent oral and written skills, strong interpersonal and listening skills
Results driven to achieve creative and sound outcomes
Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment.
Ability to make sound and timely decisions; agile in learning and action oriented
High level of emotional intelligence; able to deal with ambiguity
Able to relate to varied level audiences across the organization; able to set priorities for team and maintain accountability; skilled in negotiating organizational boundaries and hierarchy; able to build effective teams

Nice To Haves

Experience in molecular oncology and/or translational science
Medical specialty and sub-specialty training and Board Certification

Responsibilities

Serving as medical monitor with primary responsibility for patient safety and conduct of assigned trials as well as overall data interpretation and safety surveillance
Establishing and approving scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports
Assisting in design of clinical development plans and overall strategy for compounds, therapeutic classes of compounds or indications in light of developments in the area of clinical and pharmaceutical oncology
Collaborating with pre-clinical and translational sciences, and senior management in assessing requirements for emerging products
Participating in the selection and management activities of CROs
Supervising project team members in planning, conducting and evaluating clinical trials
Planning and managing investigator meetings, advisory boards and other scientific committees

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