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Job Details


Company: Docs Global (Continental Europe)
Location: Brussel,Netherlands
Reference: Ref AS-023494
Closing Date: 18 Feb 18
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

This is an exciting opportunity for motivated, experienced CRAs to make a significant contribution to the development of new medicines that will have a real benefit for patients around the world.


Roles & Responsibilities of the position

Monitoring sites in The Netherlands, but required to be in Brussels at least 3x per month, to keep in touch with the team. Expert on how to monitor in The Netherlands, sites are located from Groningen to Rotterdam, 10 sites in total.
- Study start-up preparation
- Monitoring
- Reporting and follow up
- Data Management
- Attend Monitors and Investigators meeting when organised
- Assist Project Manager in the preparation of audits and the follow-up of audit findings
The study will be risk based monitoring; every 6-8 weeks face-2-face contact, and in between monitoring by phone.
Working autonomously
Phase I experience is required
Excellent knowledge of Dutch and English

- Quality oriented!
- Flexibility – no 9-5 mentality
- Adaptability – at least 50% will be oncology, other domains are orphan disease, cardio, etc.
- Willing to travel

Job Requirements

Language: English, Dutch: very good
Good, to very good knowledge of GCP, also in practice
Good knowledge of the ‘clinical trials’ environment/regulation in the Netherlands, role of authorities, local ethics Committees, essential documents, etc
Experience as CRA (at least 2 years). NB Experience in related function eg study startup department or as in house CRA can be taken into account, but hands on experience in monitoring is required.
Basic scientific know-how, at least Bachelor, but preferably Master diploma (biomedical science, higher nursing degree, Phd or pharmacy) – if sufficient equivalent working experience, a lower degree would be acceptable (knowhow by experience)
Experience in more than 1 therapeutic domain, and oncology would be a must
Nice to have:
? French language: spoken and written (possibility to monitor French speaking Belgian sites)
? Extensive experience in oncology, as monitor or other function (nurse, study coordinator etc), knows well the oncology centers in the Netherlands; domains: solid tumors and/ or hematology (eg Leukemia, lymphoma etc)
? Experience in ‘early phase studies’
? Can present fluently and speak ‘effectively’ in Dutch and English, for eg at local investigator meeting, study initiation meeting
? Senior level, takes initiatives, issue solver, can build a long term and privileged relationship with the center research staff, is recognised as a prefered and very trustful partner, in depth diplomatic skills (important for KOL management)

Remuneration & other details

Interested? Please submit your CV to or call +31 6 42427987.

Apply for this job: Sr. CRA

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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