Senior CRA-CRA II - single sponsor, global CRO - Benelux
4 days left
- Company
- i-Pharm Consulting
- Location
- Belgium
- Salary
- Negotiable
- Posted
- 16 Feb 2021
- Closes
- 02 Mar 2021
- Ref
- YVAN013
- Contact
- Yana Vandenberghe
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
i-Pharm Consulting is seeking an experienced CRA to join a top 10 CRO and work across a range of complex therapy areas. This is an excellent opportunity to gain the skills and knowledge from a top rated training department.
LOCATION
Belgium - Home or Office Based
RESPONSIBILITIES
- Conduct site initiation visits, routine monitoring and close out visits
- Applying research regulatory requirements, GCP and ICH
- Present trial protocols at investigator meetings
- Liaise between study site personnel and the company
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.
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 / Oncology / Dutch / French / English / Belgium / België / Senior CRA / Single Sponsor / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global Pharma /
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