i-Pharm Consulting

Senior Clinical Research Associate - Netherlands

2 days left

Location
Netherlands
Salary
Negotiable
Posted
29 Nov 2018
Closes
21 Feb 2019
Ref
SCRANL65285
Contract Type
Permanent
SENIOR CLINICAL RESEARCH ASSOCIATE | PERMANENT POSITION | THE NETHERLANDS



If you are a Clinical Research Associate with more than 4 years monitoring experience and are looking for an CRA position with less monitoring required and added responsibilities, this role will be of interest to you. As an experienced CRA you will have the opportunity to take the lead on a variety of exciting trials across a broad range of therapy areas and phases of study with this leading CRO in the Netherlands. Moreover you will have a diverse role of working within the start up department as well, completing tasks (submissions, contract negotiations etc...) in the intiation period of upcoming studies. The company offer fantastic flexibility regarding work-life balance. They also implement and strategies your step by step career progression plan with you from the first day.





JOB TITLE

Senior Clinical Research Associate / Study Start Up





LOCATION

Netherlands (home/office flexibility)





BENEFITS

Generous Salary

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, site monitoring and close out visits on assigned studies across multiple therapy areas. Your role will also have responsibilities of a group of clinical staff that will include CTAs, CRAs. You will be working in a rapidly expanding part of the business with many opportunities for further career progression.





REQUIREMENTS

Life Sciences Degree or equivalent, in a scientific or healthcare discipline

4 years + monitoring experience

Experience working in a CRO or Pharma Company

Fluency in Dutch and English





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 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

CRA / CRAI / CRA II / CRA III / SSU / Study Start Up Specialist / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Clinical Research Monitor / Clinical Trial Monitor / Clinical Monitor / 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 / ICH-GCP / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Home-Based / Amsterdam / Rotterdam / Utrecht /Eindhoven/Den Haag/Maastricht/Tilburg/Groningen/ Noord Holland/ South Holland / Zuid Holland/ Noord Brabant/ Nederland

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