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CRA II / SCRA - Late Phase/Observational Studies

Business Type: Clinical Research Organisation
Job Type: Clinical Research Associate (CRA), Senior Clinical Research Associate (SCRA)
Job Level: Experienced (non manager)
Position: Full Time
Location: United Kingdom
Reference: CNOB736
Closing Date: 19/08/19
Job Details:

My client is a fast growing, international CRO that is seeking an experienced CRA to join their team and work across late phase/observational studies. The ideal candidate will have monitoring experience and will have the interest in working on late stage studies. This is an excellent opportunity to join a CRO that prides itself on its culture and looks to develop a stimulating and rewarding environment.


  • Home Based - UK Wide


  • Conduct site initiation visits, routine monitoring visits, and close-out visits
  • Liaise with the PI and site staff
  • Apply research regulatory requirements, GCP and ICH.


  • Bachelor of Science or Bachelor of Nursing Degree
  • Phase IIIb or IV experience or looking to work within late phase experience
  • 1+ years monitoring experience
  • Entitlement to work in the UK
  • Full UK drivers licence


  • Excellent Salary
  • Healthcare
  • 25 days'' annual leave
  • Pension


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 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 / North West / Scotland / Edinburgh / Aberdeen / Glasgow / South West / South East / East Midlands / West Midlands / London / Pharma''s / Major Pharma''s / Sponsor Pharma''s / CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Late Phase / Observational / Non-Interventional /

Posted: 12/08/2019 | NPJ Ref: 240120
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