Company: i-Pharm Consulting
Closing Date: 19 Jan 17
Salary (£): Negotiable
JOB SUMMARYMy client is a leading CRO with a large international presence, working with the top Pharma’s. They are seeking an aspiring CRA with 1+ years monitoring experience to join their team. This company offers excellent training and development resources and a strong management structure. With a wide range of studies this is a great opportunity for a driven CRA to develop their skills and knowledge in a range of complex therapy areas. ...
My client is a leading CRO with a large international presence, working with the top Pharma’s. They are seeking an aspiring CRA with 1+ years monitoring experience to join their team. This company offers excellent training and development resources and a strong management structure. With a wide range of studies this is a great opportunity for a driven CRA to develop their skills and knowledge in a range of complex therapy areas.
UK Wide – Home or Office Based
• Conduct site initiation visits, routine monitoring and close out visits
• Applying research regulatory requirements, GCP and ICH
• Present trial protocols at investigator meetings
• Liaise between study site personnel and the company
• Bachelor of Science or Bachelor of Nursing Degree
• 1+ years’ 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
• Bonus scheme
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 email@example.com. 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 / Manchester / Birmingham / East Midlands / West Midlands / Midlands / South West England / North West England / South East England / North East England /CRO / Contract Research Organisation / Pharmaceutical / Field Based / Office Based/ Global Pharma / Pharma Industry / Routine Monitoring / Site Initiation Visits / Close Out Visits /
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