Company: i-Pharm Consulting
Location: South West England
Closing Date: 24 Feb 17
Salary (£): Negotiable
JOB SUMMARYCRA II / SCRA Leading Midsized CRO Rapidly growingSouth West England Low number of protocols and site visits Excellent routes for progression RESPONSIBILITIES • Conduct site initiation visits, routine monitoring visits, and close-out visits • Possess strong communication skills - to present findings at investigator meetings and to discuss budgets with potential investigators• Mentor junior members of the team• Liaise with site personnel REQUIREMENTS• Bachelor of Science or Bachelo ...
CRA II / SCRA
Leading Midsized CRO
South West England
Low number of protocols and site visits
Excellent routes for progression
• Conduct site initiation visits, routine monitoring visits, and close-out visits
• Possess strong communication skills - to present findings at investigator meetings and to discuss budgets with potential investigators
• Mentor junior members of the team
• Liaise with site personnel
• Bachelor of Science or Bachelor of Nursing Degree
• 1+ years monitoring experience
• Entitlement to work in the UK
• Excellent Salary
• Bonus scheme
• 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 / CRA II / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / CNS / England / South West England / Bristol / CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Midsized CRO /
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