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CRA / SCRA - MAJOR PHARMA



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: CNOB737
Closing Date: 19/08/19
Job Details:

JOB SUMMARY

i-Pharm consulting is seeking an experienced CRA to join a top CRO where you would be outsourced to their single sponsor model, working with a major pharma. My client is looking for a CRA with 2+ years monitoring experience and who is willing to conduct 9 nationwide site visits per month. With the opportunity to progress within the company this is a chance not to be missed.

JOB LOCATION

UK Wide - 9 site visits per month

RESPONSIBILITES

  • Conduct site initiation visits, routine monitoring visits, and close-out visits
  • Implement and monitor trials across a broad spectrum of therapeutic areas
  • Adhere to GCP/ICH regulatory guidelines
  • Monitor patient safety
  • Act as the liaison between study site personnel and the company

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 2+ years UK monitoring experience
  • Experience carrying out site initiation visits and close-out visits
  • 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
  • Flexi Benefits

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 Team Leader 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 / SCRA / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / ICH / Oncology / CNS / Cardiovascular/ Paediatrics / Rare Diseases / England /South West / London / North West/ North East / Midlands / CRO / Contract Research Organisation / Pharmaceutical / Home Based / Major Pharma / Site Initiation Visit / Close Out Visit / Routine Monitoring /



i-Pharm Consulting Posted by:: i-Pharm Consulting (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 12/08/2019 | NPJ Ref: 240121
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