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
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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
Company
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