BENELUX - Senior CRA / CRA II - early phases

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.

LOCATION

Belgium - Home or office based

ROLE/DESCRIPTION

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.

REQUIREMENTS

• 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

BENEFITS

• Excellent Salary
• Company car or car allowance
• Healthcare
• Life Assurance
• 25 days' annual leave
• Pension
• 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.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Senior Consultant Yana Vandenberghe on +31 20 808 1524, or email yvandenberghe@i-pharmconsulting.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.

KEY WORDS

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 /