Associate Director

1 tydzień temu

Warszawa, Mazovia, Polska AstraZeneca Pełny etat

At AstraZeneca, we focus on fostering a collaborative culture that promotes knowledge-sharing, ambitious thinking, and innovation - giving employees the chance to work across teams, functions, and even the globe.

Our working methods prioritize individual flexibility, allowing employees to balance personal and work commitments while maintaining a culture of collaboration and teamwork by meeting face-to-face in our offices three days a week. Our head office and BlueSky Hub in downtown Toronto are designed for collaboration, providing spaces for teams to strategize, brainstorm, and work on key projects.

Our commitment to sustainability is at the core of our culture, making AstraZeneca a great place to work. We understand the interconnectedness of people's health, the planet, and our business, which is why we are taking bold actions to address significant challenges like climate change, healthcare access, and disease prevention.

Oncology Research & Development, Late Development Oncology

Our goal is to eradicate cancer as a cause of death, a vision that motivates and unites us. With various indications and high-quality molecules in our innovative pipeline, we continue to move forward by focusing on cutting-edge science and technology for breakthroughs. At AZ, we embody courage, curiosity, and collaboration - making bold decisions driven by patient outcomes.

What you'll do

The Medical Scientist plays a crucial role in the Clinical Project Team (CPT) and Global Study Team (GST), collaborating harmoniously in a matrix environment with other team members, field-based liaisons, and site personnel. Together with the Study Physician, you will work on the clinical aspects of a program, including planning, execution, recruitment, delivery of clinical studies, and providing clinical/scientific input for strategies. Responsibilities also involve contributing to protocol design, data review, interpretation, reporting, and activities for global product registration.

Other responsibilities include:

  • Work cross-functionally within clinical product teams to develop study concepts and protocols.
  • Build relationships with consultants, key external experts, and study sites for feedback and recruitment strategies.
  • Ensure clinical science integrity in studies based on detailed scientific review.
  • Provide leadership in protocol development, study reports, and medical oversight.
  • Collaborate with various functions to ensure input into protocols and governance bodies.
  • Contribute to study safety reviews, clinical data review, and governance committee interactions.
  • Participate in advisory boards for robust study designs and engagement with key experts.

Essential for the role

  • Bachelor's degree in life sciences or equivalent.
  • Experience in drug development in industry or academia.
  • Knowledge of GCP and other regulations in clinical research.
  • General understanding of medical monitoring, regulatory approvals, pharmaceutical industry operations, and oncology.
  • Demonstrated ability in clinical development planning, protocol design, and implementation.
  • Proficiency in methodology for clinical research design, conduct, review, and interpretation.

Desirable for the role

  • Advanced degree in life sciences, oncology experience.
  • Strong background in regulatory submission and leadership skills.
  • Effective communication and presentation skills for scientific concepts in team and leadership settings.

Interested in joining AZ? Discover why great people want to work with us by applying today. AstraZeneca is an equal opportunity employer dedicated to diversity, inclusion, and providing a discrimination-free workplace. We also offer accommodation for persons with disabilities upon request during the recruitment process.

Date Posted

16 May 2024

Closing Date

31 May 2024

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