BENELUX - Senior CRA / CRA II - early phases
- Experience Level
- Experienced (non-manager)
I am currently partnering a world leading CRO that is seeking an experienced CRA with 12+months experience to join their team and work across a range of therapy areas. This top CRO has an excellent development structure in place that enables CRA's to quickly progress within the company.
Belgium - Home or office based
You will conduct site initiation visits, routine monitoring visits, and close-out visits. You will also possess strong communication skills - to present findings at investigator meetings and to discuss budgets with potential investigators.
You will have previous experience building and maintaining relationships with clinical research sites.
- Bachelor of Science or Bachelor of Nursing Degree
- 1+ years independent monitoring experience
- Thorough knowledge of GCP and ICH
- Strong working knowledge of EDC systems and IVRS is desirable
- Fluent knowledge of Dutch, French and English
- Entitlement to work from home or in the office in Belgium
- Full drivers' licence
- Excellent Salary
- Company car or car allowance
- Life Assurance
- 25 days' annual leave
- Flexi Benefits
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
If you would like to discuss this vacancy further, please call Senior Consultant Yana Vandenberghe on +31 20 808 1524, or email email@example.com. If this role is not suitable, Yana is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / CRA II / Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Dutch / French / English / Belgium / Senior CRA / Core Clinical / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global Pharma /