CRA - reduced monitoring - RWE - Belgium

i-Pharm Consulting
Closing date
18 Sep 2020

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Clinical Research, Clinical Research Associate
Full Time
Contract Type
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Clinical Research Associate - Reduced monitoring - Belgium


IQVIA is seeking an experience trilingual CRA to work on their Real world Evidence studies in the later phase. Real world data comes into place when Clinical trials cannot account for the entire population of a disease. This position is home or office based in Belgium with a lot of remote monitoring. This is an exceptional opportunity for CRAs with 6 months' of independent experience to work within a Global CRO on future oriented studies




  • Routine onsite monitoring
  • Organising and managing research projects with contribution to study protocols , reports and data collection methods.
  • Conducting pre-study and initiation visits as well as close-out clinical sites
  • Organising and making presentations at Investigator Meetings
  • Participation in development of assigned protocols
  • Negotiate study budgets with potential investigator


This CRO is a visionary leader in the pharmaceutical industry, with training and career development high on their list of priorities. This company has a growing network of 50,000+ employees operating in over 110 countries globally. Trials are ongoing in a broad range of therapeutic areas including: , Oncology and infectious diseases.


  • Bachelor of Science or Bachelor of Nursing Degree
  • 6+ months of independent monitoring experience
  • Willingness to perform Remote monitoring
  • Willingness to perform site visits.
  • Thorough knowledge of Good Clinical Practice (GCP)
  • Entitlement to work in the Belgium
  • Trilingual : English and French Dutch
  • Full Belgian drivers licence


  • Reduced Monitoring (2- 3 site visits a month)
  • Car or car allowance
  • Healthcare
  • 25 days' annual leave
  • Pension
  • Flexi Benefits


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.


If you would like to discuss this vacancy further, please call Recruitment Consultant Jasween Kaur on +31 (0)20 8081497, or email If this role is not suitable, Jasween is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


CRA / CRA II / Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / Cardiovascular / Ophthalmology / Infectious Disease / Respiratory / Women's Health / Belgium / CRO / Contract Research Organisation / Pharmaceutical / Home Based

Life Sciences recruitment is what we do.

We are an award-winning international life sciences recruitment company with offices in London, New York, Munich, Singapore and Sydney.  In a highly competitive market-place, we connect top talent with the very best opportunities.


Our clients include many of the most successful and innovative Pharmaceutical, Biotechnology, and Medical Devices companies, as well as a range of Contract Research & Manufacturing Organisations, Healthcare Agencies and Consultancies.


With offices across 3 continents, we have teams servicing the major global life science hubs. We combine local knowledge, with a global network of contacts that allows us to bring together talent and opportunity when it matters most.

Contact Us
  • 212 New King’s Road
  • London
  • SW6 4NZ
  • GB
  • +44 (0) 20 3189 2299
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