Local Study Associate Director Oncology
Local Study Associate Director Oncology
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Job Description
Are you ready to make a difference with your expertise in a company that transforms scientific ideas into lifechanging medicines At AstraZeneca we harness the potential of our people encouraging you to exceed your expectations and achieve remarkable outcomes.
Join us at MIND (Milan) one of our vibrant sites where collaboration and authenticity are key. As a global scienceled biopharmaceutical company we focus on improving patient health worldwide fostering innovation to develop groundbreaking medicines. With an unparalleled product portfolio in Oncology Respiratory and CardioRenal Metabolic diseases we invite you to lead Local Study Teams (LSTs) at the country level delivering clinical studies with precision and compliance.
Are you inspired by sciences possibilities Discover what you can achieve with us!
Accountabilities
As the Local Study Associate Director you will oversee clinical studies at the country level ensuring successful execution from site identification to documentation archiving. Your leadership will drive operational management compliance and relationship management for highquality study data delivery. Key responsibilities include:
Leadership and Oversight: Lead Local Study Team (LST) optimize team performance ensure compliance organize meetings and manage budgets.
Study Management: Meet study commitments develop monitoring plans coordinate site selection and ensure timely document submissions.
Monitoring and Compliance: Perform comonitoring visits review reports and oversee audit activities.
Documentation and Systems: Ensure document completeness maintain systems and prepare for final archiving.
Collaboration and Reporting: Work closely with CRAs Investigators Regulatory Affairs and provide updates on progress.
Training and Support: Train new team members and contribute to process improvements.
Miscellaneous: Ensure compliance with company values and support regional initiatives.
Essential Skills/Experience
University degree or equivalent preferred in biological science or healthcarerelated field
Minimum 1 yearexperience as Project Manager in Clinical Operations
A previous experience as CRA
Fluent knowledge of spoken and written English and Italian
Excellent knowledge of international guidelines ICH GCP
Good knowledge of relevant local regulations
Good medical knowledge in Oncology Therapeutic Area
Excellent knowledge in Clinical Operations and understanding of the Clinical Study Process
Excellent knowledge/experience of the Monitoring Process
Good understanding of the Study Drug Handling Process and Data Management Process
Leadership capabilities
Excellent project management and organizational skills
Goals oriented
Ability to manage several complex projects at the same time
Domicile: Milan
When we put unexpected teams in the same room we unleash bold thinking with the power to inspire lifechanging medicines. Inperson working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
AstraZeneca offers an environment where collaboration and learning are integral to our success. We work together across locations and therapy areas to share knowledge and unlock opportunities for personal and professional growth. Our innovative approach in Oncology Regulatory ensures rapid approvals transforming breakthrough science into tangible value for patients. Here youll be empowered to take ownership of your work and thrive in a diverse and inclusive setting.
Ready to step up and make a difference Apply now to join our dynamic team!
Date Posted
09mag2025Closing Date
23mag2025AstraZeneca 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 industryleading 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 nondiscrimination in employment (and recruitment) as well as work authorization and employment eligibility verification requirements.
Required Experience:
Director
Employment Type
Full-Time
