CRA II/ Senior Clinical Research Associate

Location
England
Salary
Negotiable
Posted
19 Jul 2019
Closes
02 Aug 2019
Ref
HGSCRA990
Contact
Hannah Scheel
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

JOB SUMMARY

CRA II/ SCRA

Niche CRO

London

Working across Oncology and Immunology trials

RESPONSIBILITIES

  • Conduct site initiation visits, routine monitoring visits, and close-out visits
  • Possess strong communication skills - to present findings at investigator meetings and to discuss budgets with potential investigators
  • Mentor junior members of the team
  • Liaise with site personnel

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 1.5 + years independent monitoring experience
  • Entitlement to work in the UK
  • Eligibility to work in the UK
  • Valid driving licence

BENEFITS

  • Excellent Salary - £34,000 - £55,000
  • Bonus scheme
  • 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 Hannah Scheel on +44 (0)20 3189 2296, or email hscheel@i-pharmconsulting.com. If this role is not suitable, Hannah is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

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 / Immunology/ England / London/ CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global CRO

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