Umowa o pracę - Enablement Assistant (Trial Master File Enablement Activity)
AstraZeneca Pharma Poland Sp z o.o. Postępu 14, Postępu, Warszawa, Polska 13 września 2018

At AstraZeneca we are guided in our work by a strong set of values, and we’re resetting expectations of what a bio-pharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicinesthat transform lives. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. If you’re interested in developing medicines and curious about what science can do, then you’re our kind of person.

Umowa o pracę - Enablement Assistant (Trial Master File Enablement Activity)

is a member of the Clinical Operations Enablement Team, and is actively supporting Clinical Operations by ensuring the population and availability of complete, high quality data from Clinical Operations processes and systems.

Individuals in this job may be assigned one or more roles relating to the development and maintenance of Enablement processes, systems and services owned by GMD Clinical Operations.


As the member of a specific activity team Enablement Assistant:

  • Supports Enablement services across drug projects
  • Maintains systems/tools and data associated with Clinical Operations enabling services in partnership with Study Teams and external partners to appropriate standards, completeness, quality and consistency
  • Supports life cycle management and business continuity for Clinical Operations processes, systems/tools, standards, procedural documentation and training materials
  • Provides support to user communities including: conducting relevant process/system; preparing communication within Clinical Operations; taking part in validation and testing of processes and systems
  • Contributes to business cases for continuous improvement project
  • Participates in change initiatives relating to Clinical Operations.
  • Supports activities that ensure Clinical Operations compliance
  • Works with teams and colleagues across the organization to support consistent ways of working and adherence to best practice


  • Familiarity with eTMF systems is desirable
  • Communicative English (fluent is desirable)
  • Proven organizational and analytical skills
  • Display the ability to follow tasks through to completion and to understand how tasks combine into an efficient workflow
  • Demonstrated concern for quality and standards, good team-working
  • Computer proficiency
  • Good time management
  • Strong communication skills


  • Experience related to clinical trials documentation management
  • Work experience in the pharmaceutical industry or in the environment of clinical study delivery/clinical development processes
  • Knowledge of pharmaceutical drug development and clinical study processes and associated government regulations, ICH GCP.


  • Employment contract
  • Benefits package

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CV in English