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Clinical Research Associate Milan, Lombardy, Italy

AstraZeneca
Milan, Lombardia
4 giorni fa

Location Milan, Lombardy, Italy

Job ID R-231978

Date posted 20/07/2025


Are you ready to make a difference in patients' lives through groundbreaking science? At AstraZeneca, we believe in the potential of our people and support you to achieve beyond your expectations.

As a Clinical Research Associate (CRA) in Italy, you will be at the forefront of scientific innovation, playing a crucial role in delivering studies at allocated sites and actively participating in local study teams.

Join us in our mission to uncover new mechanisms and develop targeted therapies that transform treatment for today's diseases. If you're inspired by the possibilities of science and eager to explore what you can achieve, this is your opportunity!

Accountabilities
As a CRA, you will report to the Director SMM and collaborate closely with other CRAs and the Local Study Team/Local Study Associate Director. Your responsibilities include monitoring study conduct, ensuring compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. You will drive performance at study sites, resolve study-related issues, and ensure timely reporting of Serious Adverse Events. Your role encompasses site selection, initiation, monitoring, closure, and collaboration with local MSLs. You will manage study supplies, perform monitoring visits, and prepare for audits and regulatory inspections. Your commitment to quality and compliance will ensure successful study delivery.

Essential Skills/Experience
  • Scientific Degree equivalent degree
  • Experience as CRA in a pharma company or CRO
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
  • Good knowledge of relevant local regulations
  • Good medical knowledge and ability to learn relevant AZ Therapeutic Areas
  • Basic understanding of the drug development process
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management
  • Excellent attention to details
  • Good written and verbal communication skills
  • Good collaboration and interpersonal skills
  • Good negotiation and problem-solving skills
  • Ability to travel nationally/internationally as required
  • Valid driving license
  • Preferred location: Milan and surroundings
Desirable Skills/Experience
  • Demonstrated project management skills including scope, budget, timeline, resource management and use of associated tools
  • Experience from Clinical Research/Operations (i.e., hands-on work with Clinical Trial Management in the pharmaceutical industry)
  • Knowledge of R&D ways of working
  • Ability to effectively work with External Service Providers
  • Ability to look for and champion more efficient and effective methods/processes

AstraZeneca is driven by the solutions we bring to the healthcare ecosystem, making an impact at every step of the patient journey. We thrive on energy and pace, fostering a winning mentality that propels us forward. Our inclusive team draws on diverse backgrounds to create innovative solutions that improve patient experiences and outcomes. With countless opportunities for growth, AstraZeneca is where top talent shapes the future of BioPharmaceuticals.

Ready to join us on this exciting journey? Apply now and be part of a team that's transforming healthcare!

Date Posted

21-lug-2025

Closing Date

27-lug-2025

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.

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