Senior CRA-CRA II - single sponsor, global CRO - Benelux

4 days left

Location
Belgium
Salary
Negotiable
Posted
16 Feb 2021
Closes
02 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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