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Clinical Research Associate II (BE)

22.02.2019 REF: O190018 Flemish Brabant

Organization

CRO

Description of the Position

In this position you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if applicable)
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Demands of the Position

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Experience of 2 years independent on-site monitoring in Belgium
• Experience in all types of monitoring visits in Phase II and/or III
• Full working proficiency in English, Dutch and French
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

Terms of Employment

Directly at the clients headcount.
Interested in this challenge?! For more information, feel free to contact Nick Dufour at 0032 (0)475 87 02 36 or n.dufour@theclinicalcompany.com or apply directly.

Nick for Belgium

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+32 475 87 02 36n.dufour@theclinicalcompany.com

Simone for the Netherlands

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+316 12996359simone.polman@theclinicalcompany.com

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