About the Company
Our client, a leading player in the clinical research market, is currently seeking Clinical Research Associates to support long term sponsors across Belgium. Projects are within Flu studies. This would be based on a 6 month freelance contract and ideally on a 1.0 FTE although slightly reduced FTE can be considered also.
About the Role
As a Clinical Research Associate, you will have the opportunity to work on challenging projects as part of a multinational team, delivering exceptional customer service. Providing long-term value is paramount to my client and you will get a good work-life balance and career exposure.
Responsibilities
* Coordinating and performing all aspects of the clinical monitoring process.
Qualifications
* At least 3 years of on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation.
Required Skills
* Strong understanding of ICH-GCP, EU, and FDA requirements.
* Excellent communication and interpersonal skills.
Preferred Skills
* Solid knowledge of medical/therapeutic areas and terminology.
Pay range and compensation package
Our client offers award-winning training programs to enhance your technical and professional skills.
Equal Opportunity Statement
Our client is committed to diversity and inclusivity.