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Administration Assistant / Secretary in Clinical Research (f/m) – office based in Breda

Employer
IQVIA
Location
Capelle a/d IJssel
Start date
23 Jul 2019
Closing date
22 Aug 2019

View more

Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
Experience Level
Entry level

Job Details

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

You have working experience in the administrative field e.g. as a secretary? You would like to start your career in clinical research? – This is the perfect opportunity for you!

We are currently looking for a Clinical Trials Assistant / Secretary (f/m) in the pharmaceutical field, to work on the administration of Dutch clinical trials office based in Breda.

Your typical responsibilities might include:

  • Support of the project team with the planning, organization and documentation of various clinical trials
  • Acting as the interface between the clinical researchers (CRAs) and the project management
  • Creating study relevant documents and reports, taking over data management tasks in different databases and coordinating the internal communication

You should have:

  • High / Secondary School diploma or country’s educational equivalent (MBO/HBO)
  • Working experience in an administrative job e.g. as a secretary
  • Good written and verbal communication skills including good command of Dutch and English language
    Good computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
  • Effective time management and organizational skills
    Ability to establish and maintain effective working relationships with co-workers, managers and clients.
  • Preferably awareness of clinical research regulatory requirements; e.g., Good Clinical Practice (GCP) guidelines

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

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