Clinical Research Associate II/ Senior CRA - Netherlands
4 days left
- Experience Level
- Experienced (non-manager)
This leading international CRO is seeking a CRA II to work onsite with a global pharma sponsor. This is an excellent opportunity to work with a single sponsor on multiple therapy areas including oncology. This is a great opportunity for CRAs with 1+ years' independent monitoring experience to work with a global pharma sponsor that is well recognised in the industry and has a proven route of progression.
Netherlands - Home or office based
You are expected to have +1 year of experience as a CRA or Sr CRA 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.
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 and English
- Entitlement to work from home or in the office in 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 Tim Lobley on +44 (0) 2039071986, or email email@example.com. If this role is not suitable, Tim 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 / NL / Netherlands / Nederland
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