Company: i-Pharm Consulting
Closing Date: 20 Jan 17
Salary (£): Negotiable
JOB SUMMARYSeeking a CRA with 1+ years’ monitoring experience to join a leading CRO. This is a single sponsor model and therefore you will work directly with a top pharma. This role involves regional monitoring and therefore offers a great work-life balance. ...
Seeking a CRA with 1+ years’ monitoring experience to join a leading CRO. This is a single sponsor model and therefore you will work directly with a top pharma. This role involves regional monitoring and therefore offers a great work-life balance.
Berkshire – regional monitoring
• Work directly with the sponsor across a large spectrum of therapeutic areas
• Apply research regulatory requirements, GCP and ICH
• Liaise with PI’s and site staff
• May be required to act as a mentor to members of the clinical research team and assist them in their training and development
• Bachelor of Science or Bachelor of Nursing Degree
• 1+ years independent monitoring experience
• Experience working in a range of therapeutic areas
• Sound presentation and communication skills
• Entitlement to work in the UK
• Full UK Driver’s License
• Excellent Salary
• Car allowance
• 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 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 / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / England / London / Maidenhead / CRO / Contract Research Organisation / Pharmaceutical /Single Sponsor / Home Based / Pharma / Top Pharma / Outsourced /
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