CRA II / Senior CRA - UK - Reduced Travel

2 days left

Location
England
Salary
Negotiable
Posted
01 Jun 2021
Closes
15 Jun 2021
Ref
CNOB838
Contact
Ciara Noble
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

This leading midsize CRO with a strong international presence is seeking an experienced CRA who has worked with complex studies across a range of therapeutic areas, including Oncology. This is an excellent opportunity for a CRA with 2+ years' experience to work with the top pharma sponsors and help contribute to the development of life changing drugs.

LOCATION

England - Home Based

4/5 visits per month

RESPONSIBILITIES

  • Conduct site initiation visits, routine monitoring visits, and close-out visits
  • Independently ensuring sites are monitored in accordance with protocol monitoring guidelines, GCP and ICH guidelines
  • Develop and maintain relationships with investigational sites and client company personnel.
  • Monitor patient safety
  • Data collection
  • Presenting trial protocols at investigator meetings

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 2 years independent monitoring experience
  • Experience working in a range of therapeutic areas
  • Entitlement to work in the UK

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 Business Manager 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 / International Conference on Harmonisation guidelines / ICH / Oncology / Neuroscience / Cardiovascular/ Paediatrics / Women's Health / Endocrine & Metabolic / Rare Diseases / England / Scotland / Wales / London / CRO / Contract Research Organisation / Pharmaceutical / Home Based / Major Sponsors / Multiple Sponsors / Site Initiation Visits / Close Out Visits / Routine Monitoring / England /

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