Company: i-Pharm Consulting
Location: South East England
Closing Date: 26 Oct 16
Salary (£): Negotiable
JOB SUMMARY This leading international CRO is seeking a CRA with 2+ years’ experience to join their team and to work across a range of therapy areas for a top Pharma. As this is a Single Sponsor model it offers a great work-life balance with regional monitoring. This is a great opportunity for a motivated CRA to join a company that looks after the well-being of their employees. ...
This leading international CRO is seeking a CRA with 2+ years’ experience to join their team and to work across a range of therapy areas for a top Pharma. As this is a Single Sponsor model it offers a great work-life balance with regional monitoring. This is a great opportunity for a motivated CRA to join a company that looks after the well-being of their employees. This CRO will provide the opportunities needed to succeed in the industry and to help you develop your professional career.
UK Wide – Regional Monitoring
• Implement and monitor trials across a broad spectrum of therapeutic areas including Oncology
• Conduct site initiation visits, routine monitoring and close out visits
• Applying research regulatory requirements, GCP and ICH
• Liaise between study site personnel and the company
• Bachelor of Science or Bachelor of Nursing Degree
• 2+ years UK monitoring experience
• Competent in written and oral English
• Entitlement to work in the UK
• Full UK drivers licence
• Excellent Salary
• Car allowance or Car
• 25 days’ annual leave
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 Recruitment Consultant Ciara Noble on +44 (0)20 31890469, or email firstname.lastname@example.org. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / Clinical Research Associate / CRA II / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / Cardiovascular / Ophthalmology / Rheumatology / London / South East / South East England / North East England / North West England / East Midlands / West Midlands / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Field Based / Office Based/ Global Pharma / Single Sponsor / Pharma Industry / Routine Monitoring / Site Initiation Visits / Close Out Visits /
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