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An experienced CRA is required to join a niche CRO. The role will be based in Scotland (between Edinburgh and Stirling) and will be at least partly office-based. Applicants should have a minimum of 12 months clinical monitoring experience.
CRA / Clinical Research Associate - Central Belt Scotland
You'll be joining a specialist Drug Development Services Company working on a range of projects across Phases II-IV in the field of CNS. This company monitors studies in the UK, Europe and the US, so is a great opportunity to gain global exposure.
Monitor clinical trials in accordance with ICH-GCP standards, monitoring study sites UK-wide
Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
Develop, review and edit clinical trial related
Assist with study protocol design, development and / or review if required
Excellent career development prospects with a genuinely forward-thinking organisation
Generous salary and benefits package
Life sciences degree OR nursing qualification
12 months + experience as a CRA
If you would like to discuss this vacancy further, please call Principal Consultant Andy Yaxley on +44 (0)20 3189 2296, or email email@example.com. If this role is not suitable, Andy is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
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.
Clinical Research Associate / CRA / Monitoring / Scotland / Edinburgh / Glasgow / Office based / Niche / CNS / Global / Home Based / CRO