i-Pharm Consulting

Clinical Research Associate - Belgium

Location
Belgium
Salary
Negotiable
Posted
08 Dec 2018
Closes
16 Feb 2019
Ref
CRAB4548
Contract Type
Permanent
CLINICAL RESEARCH ASSOCIATE | OUTSOURCED POSITION | BELGIUM



CRA II required for new positions within a CRO and/or global Pharma if you choose to be outsourced. If you are a Clinical Research Associate with monitoring experience and are looking for a new challenge we can offer a generous salary and package, flexible working arrangements (home or office based) with training and career development opportunities. Various new studies and therapeutic areas on exciting new projects.



JOB TITLE



Clinical Research Associate / CRA II



LOCATION



Belgium





BENEFITS



Generous Salary

13th month and holiday allowance bonuses

Performance based bonus

Company car or Car allowance

Full Benefits Package

Industry leading training programmes with excellent ongoing career progression opportunities.



ROLE/DESCRIPTION



You will be involved in study start-up, site initiation, qualification visits, feasibility research, site monitoring and close out visits on assigned studies across multiple therapy areas.

You will be working in a rapidly expanding part of the business with many opportunities for further career progression.





REQUIREMENTS



12 months plus monitoring experience

Life Sciences Degree or equivalent, in a scientific or healthcare discipline would be nice to have

Experience working in a CRO, Medical Devices or Pharma Company is desirable

Fluency in English, Dutch and French (flexible)







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 Benelux Clinical Operations Consultant Mak Ishola on +32 (0)2 808 2151, or email mishola@i-pharmconsulting.com. If this role is not suitable, Mak is also available to discuss other possible positions or answer any general questions regarding your career and the current market.



KEY WORDS

Clinical Research Monitor / Clinical Site Monitor / Senior Clinical Site Monitor / CSM / Senior CSM / Sr CSM / CRA / CRA I / CRA II / SSU / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research / Clinical Trials / Study Start-Up / Start-Up / Study Start Up / SSU / Clinical Study Start-Up/ Regulatory Affairs / Regulatory Documents / Regulatory Submissions / Ethical Submissions / ICH-GCP / GCPv / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Home-Based / Antwerpen / Aalst / Turnhout / Mol / Mechelen / Mons / Leuven / Hasselt /Genk /Brussels / Louvain La Neuve /Lier / Overpelt / Lommel / Duffel / Ninove / Braine l'alleud / Wavre / Liege / Namur / Charleroi / Dinant / Dendermonde / Gent / Belgium

Similar jobs

Similar jobs