Clinical Research Associate

Job description:
- Selecting, preparing, guiding and monitoring of clinical investigational sites.
- Distributing and collecting all required critical documents.
- Regulatory submission to Ethics Commitees and Competant Authorities.
- Communication with clients, project manager and lead CRAs
- Taking care of quality of clinical data.
- Organisation, coordination and management of clinical sites and trials according to ICH/GCP and local requirements.

Profile:
- A minimum of 1 to 2 year CRA experience required.
- Fluent knowledge of Dutch, French and English is mandatory.
- Strong communicative and social skills.
- Can operate independently.
- Eager to incorporate the Clinitude Guiding Principles.
- Medical or paramedical degree is a surplus.

Benefits:
- a competitive salary and expense reimbursements.
- a company car + navigation system.
- group insurance + pension plan.
- mobile phone and laptop.
- free healthy snacks.
- on-site massage therapy.
- an open atmosphere and great people to work with are just part of what make us unique.