CRA II, family-feel work environment in Benelux

Location
Belgium
Salary
Negotiable
Posted
23 Feb 2021
Closes
09 Mar 2021
Ref
YVAN013
Contact
Yana Vandenberghe
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

i-Pharm Consulting is seeking an experienced CRA to join a top 10 CRO and work across a range of complex therapy areas. This is an excellent opportunity to gain the skills and knowledge from a top rated training department.

LOCATION

Belgium - Home or Office Based

RESPONSIBILITIES

  • Conduct site initiation visits, routine monitoring and close out visits
  • 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 independent monitoring experience
  • Thorough knowledge of GCP and ICH
  • Strong working knowledge of EDC systems and IVRS is desirable
  • Fluent knowledge of Dutch, French and English
  • Entitlement to work from home or in the office in Belgium
  • Full drivers' licence

BENEFITS

  • Excellent Salary
  • Company car or car allowance
  • Healthcare
  • Life Assurance
  • 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 Senior Consultant Yana Vandenberghe on +31 20 808 1524, or email yvandenberghe@i-pharmconsulting.com. If this role is not suitable, Yana 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 / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / Dutch / French / English / Belgium / België / Senior CRA / Single Sponsor / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global Pharma /

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