Senior CRA - Core Clinical - Benelux
- Experience Level
- Experienced (non-manager)
This award winning CRO is seeking an experienced CRA who has worked on complex studies across a broad range of therapeutic areas. This is a sound opportunity for CRAs with 1+ years' experience to work with a global CRO that thrives on its strong relationships with clinical research sites.
Belgium - Home or office based
You'll have experience working across study site monitoring including routine monitoring, maintenance of study files, conduction of pre-study and initiation visits and close-out of clinical sites. You will have previous experience building and maintaining relationships with clinical research sites.
You'll be responsible for organising and making presentations at Investigator Meetings, to participate in in the development of assigned protocols and Case Report Forms, and to negotiate study budgets with potential investigators. This position requires you to be involved in the study start up and close down. You will also possess strong communication skills and be confident in presenting studies.
This CRO is a visionary leader in the pharmaceutical industry, with training and career development high on their list of priorities. This company has a growing network of 25,000+ employees operating in over 45 countries globally. Trials are ongoing in a broad range of therapeutic areas.
- 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 / English / 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 / Nederland / The Netherlands