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Lieu: Hod Hasharon, Central District, Israël
ID de l'offre 13173161
Date de publication: 09/01/2019

Job Description

At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe. As a Clinical Study Administrator in Israel, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. GMD (Global Medicines Development) drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them.

The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives.

Assists in coordination and administration of clinical studies from the start-up to execution and close-out.

Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents.

Serves as local administrative main contact and works closely with the CRAs and/or the Local SM for the duration of the study.

document tracking in accordance with ICH- GCP and local requirements.

Manages and contributes to coordination and tracking of study materials and equipment.

Coordinates administrative tasks during the study process, audits and regulatory inspections, according to company policies and SOPs.

Ensures compliance with AstraZeneca’s Code of Ethics and company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).

Ensures compliance with local, national and regional legislation, as applicable.

Minimum Requirements:

  • University degree, that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
  • Previous administrative experience preferably in the medical/ life science field.
  • Proven organizational and administrative skills.
  • Computer proficiency.
  • Good knowledge of spoken and written English

Preferred Skills:

University degree Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH-GCP guidelines. Good verbal and written communication. Excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities. Team oriented and flexible; ability to respond quickly to shifting demands

Next Steps – Apply today!

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.  AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

Clinical Study Administrator
Développement clinique

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