Clinical Research Associate

Location
Belgium
Salary
On application
Posted
18 Mar 2021
Closes
17 Apr 2021
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

I am working with a global CRO who is looking for an experienced CRA to join their CNS Team in Belgium.

Responsibilities:

  • Performs all types of monitoring visits: site qualification, site initiation, interim monitoring, site management and close-out visits
  • Adherence to GCP, ICH guidelines and local regulations, and internal policies across monitoring visits
  • Supervise the conduct of clinical studies, ensure compliance with protocols, regulatory requirements, and good clinical practice
  • Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness
  • Provide county-specific expertise to ensure operational compliance with local regulations
  • Work effectively with other departments and levels within the organisation

Requirements:

  • Scientific degree/education preferred
  • Experience with monitoring in Belgium
  • Fluent in English, French and Dutch
  • Experience in one of the following indications: CNS, neurology, ophthalmology
  • Ability to manage required travel of up to 75% on a regular basis
  • Able to drive a car and have a valid driver’s license – as required

If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: roxanna.keshavarz@rbwconsulting.com / +44 1273 952187

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