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Job Details
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CRA II/SCRA I - Midlands- Regional Monitoring



Business Type: Pharmaceutical Company, 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: CNOB704
Closing Date: 16/04/19
Job Details:

JOB SUMMARY

My client is a specialist in drug development and is seeking an experienced CRA to join their team. This is an outsourced model and therefore you will work directly with a single, leading pharmaceutical company. With training and development from both a top CRO and a top pharma this is an excellent opportunity for a CRA to develop their career within the industry. As this role offers regional monitoring it ensures a better work-life balance.

LOCATION

The Midlands - Regional Monitoring

RESPONSIBILITIES

  • Working directly with the sponsor you will implement and monitor trials across a broad spectrum of therapeutic areas
  • Applying research regulatory requirements, GCP and ICH
  • Present trial protocols at investigator meetings
  • Liaise between study site personnel and the company

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 1+ years UK monitoring experience
  • Competent in written and oral English
  • Entitlement to work in the UK
  • Full UK drivers licence

BENEFITS

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

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.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Recruitment Consultant Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.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.

KEY WORDS

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 / UK / England / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Field Based / Office Based/ Global Pharma / Single Sponsor / Pharma Industry / Routine Monitoring / Site Initiation Visits / Close Out Visits / Neurology /Midlands / East Midlands / West Midlands



Posted: 09/04/2019 | NPJ Ref: 233443
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