Clinical Research Associate
il y a 1 semaine
As a successful Clinical Research Associate (CRA) - Brussels, you will have the following responsibilities:
Study Preparation:
- Support the design and the development of clinical trial protocols
- Collect and submit documentation for Board approval
- Coordinate the preparation of trial- specific training materials
Site Management:
- Select and monitor clinical trial sites with respect to the sturdy protocol and regulatory requirements
- Ensure follow-up with the clinical trial sites from A to Z : from site selection to close-out studies
Data Management:
- Review the accuracy and the completeness of case reports forms, documentation, activities and data
- Identify, follow-up and resolve data discrepancies
Compliance and Safety:
- Ensure compliance to regulatory guidelines
- Monitor, reports and follow-up any adverse events with respect to the regulatory requirements
- Conduct risk assessments and propose corrective and preventive actions if needed
As a successful Clinical Research Associate (CRA) - Brussels, you have the following requirements:
- Master Degree in Life Sciences, pharmacy or related fields
- +2 years of experiences as a Clinical Research Associate (CRA) in the pharmaceutical, biotechnology or CRO industry
- Experiences in phase I-IV studies
- Knowledge in regulatory requirements: FDA ...
- Strong organizational and time management skills
- Excellent attention for details
- Strong written and verbal communication skills
- Fluent in English, French and/or Dutch being a plus
As a successful Clinical Research Associate (CRA) - Brussels, you will have:
- A competitive salary including a package of extra legal benefits
- The chance to join a stable company proposing growing possibilities
- The possibility to join a multicultural supportive team with a nice team spirit
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