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Job Details

Global Clinical Trials Submissions Specialist

Company: i-Pharm Consulting
Location: Belgium
Reference: SSUBE01/12
Closing Date: 15 Dec 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

CRA I/CRA II/CRA II (Sr CRA) required for new positions with a global Pharma. 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. The client are looking for an array of experiences ranging from no independent monitoring experiences all the way to supervising junior CRA’s. ...

Requirements:

CRA I/CRA II/CRA II (Sr CRA) required for new positions with a global Pharma. 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. The client are looking for an array of experiences ranging from no independent monitoring experiences all the way to supervising junior CRA’s.

JOB TITLE
CRA I/ CRA II / Senior Clinical Research Associate / SCRA

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.
Your role will also include management 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. National and international travel is an integral part of this role.


REQUIREMENTS
Life Sciences Degree or equivalent, in a scientific or healthcare discipline
2 years + monitoring experience
Experience working in a CRO or Pharma Company is desirable
Fluency in English (other European language is a bonus)



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
CRA / CRAI / 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 / ICH-GCP / GCPv / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Home-Based / Antwerpen / Mechelen / Leuven /Hasselt /Genk /Brussels /Louvain La Neuve /Lier / Aalst /Dendermonde / Gent / Belgium

Apply for this job: Global Clinical Trials Submissions Specialist

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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