Senior Clinical Research Associate / II - België
- Experience Level
- Experienced (non-manager)
The role of the Senior Clinical Research Associate (CRA) is to support several ongoing and upcoming clinical trials with a global sponsor. This is an excellent opportunity to work with a single sponsor on multiple therapy areas. The position will monitor patient recruitment, enrolment, data and study-related information related to clinical trial sites and study participation. Ensures the investigators adhere to the established clinical protocols, regulatory requirements and Good Clinical Practice, and provides input into data validation.
Belgium - Home or office based
You are expected to have +1 year of experience as a Senior CRA of CRA II including the ability to interact effectively with investigators and cross-functional teams. Leadership skills and participation in a management team are key aspects of the position. You can demonstrate comprehensive and current knowledge in relevant therapeutic or product areas and possess an excellent command of medical and scientific areas assigned. 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.
With more than 65,000 employees, this world leader in using data, technology, advanced analytics and expertise works to make a positive difference in global healthcare. They focus on wellness and safety, product innovation, environmental responsibility and ethical business practices is central to their success.
- 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 The Netherlands
- 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 / Oncology / Dutch / English / French / 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 / Belgium / Belgie