Clinical Research Associate II - Niche CRO - London

Location
England, London
Salary
Negotiable
Posted
18 Jul 2019
Closes
01 Aug 2019
Ref
CNOB719
Contact
Ciara Noble
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Opportunity for a CRA with 2+ years' experience to join a growing global CRO based in London. The position will be partially office based in Central London. This is an excellent role for a CRA with previous experience in complex studies including but not limited to Oncology, Haematology and Rare Disease.

RESPONSIBILITIES

  • Working directly with the sponsors you will implement and monitor trials across Ophthalmology studies
  • 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
  • 2+ years monitoring experience
  • Competent in written and oral English
  • Entitlement to work in Ireland
  • Full drivers licence

BENEFITS

  • Excellent Salary
  • 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 / Ophthalmology / Rheumatology / England / United Kingdom / Contract Research Organisation / Pharmaceutical / Sponsor / Field Based / Office Based/ Global Pharma / Single Sponsor / Pharma Industry / Routine Monitoring / Site Initiation Visits / Close Out Visits / London

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