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Job Details

Clinical Research Associate (sponsor dedicated)

Company: i-Pharm Consulting
Location: Belgium
Reference: SPONSCA
Closing Date: 23 Feb 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

CLINICAL RESEARCH ASSOCIATEExperienced Clinical Research Associate required for new positions. 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. ...

Requirements:

CLINICAL RESEARCH ASSOCIATE

Experienced Clinical Research Associate required for new positions. 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 I/ CRA II /

LOCATION
Belgium


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


REQUIREMENTS
2 years plus independent monitoring experience
Life Sciences Degree or equivalent, in a scientific or healthcare discipline would be nice to have
Experience working in a CRO or Pharma Company is desirable
Fluency in English, Dutch or/and French



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 Principal Consultant Mak Ishola on +44 (0)20 3189 0487, 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 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

Apply for this job: Clinical Research Associate (sponsor dedicated)

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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