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Job Details

Study Start Up/Submission Specialist

Company: i-Pharm Consulting
Location: Belgium
Reference: SUBBE28111
Closing Date: 12 Dec 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

A global CRO areas is looking for a Submission Specialist or Study Start-up Associate to join their team in the Belgium. This international CRO is one of the top 10 in the whole market and is looking for ambitious candidates who are willing to join a new challenge for their career. ...

Requirements:

A global CRO areas is looking for a Submission Specialist or Study Start-up Associate to join their team in the Belgium.
This international CRO is one of the top 10 in the whole market and is looking for ambitious candidates who are willing to join a new challenge for their career.

JOB TITLE
Study Start-up Associate – Submissions Specialist – SSU

LOCATION
Belgium

SALARY & BENEFITS
Very Competitive Salary package + Benefits
+13th month
+Car or Car allowance
+Reimbursement of Mileage
+Pension
+Healthcare
+Life insurance
+Meal vouchers

ROLE/DESCRIPTION
In charge of different regulatory submissions as well as the preparation and review of local ethics.
To work directly with local regulatory authorities.
Will be the key person on the country level for the submission and all the oversight of the projects.
Make, review and keep track of contracts using the legal and commercial knowledge.
Additional Tasks would performed according to departmental needs.

REQUIREMENTS
Life Sciences Degree or equivalent, in a scientific or healthcare discipline
Regulatory experience and/or submissions experience
Vast knowledge of the local requirements for submissions
Experience working in a CRO or Pharma Company
Fluency in French, 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 the Benelux 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 / CTA / CRAI / CRA II / SSU / Senior CRA / SCRA / Submission Specialist / Global Trials Submissions Specialist / Global Clinical Trials Submissions Specialist / GCTSS / GCSS / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research /Central Europe /Brussels / Gent / Antwerpen Genk / Namur / Charleroi / Dinant / Mons / Hasselt / Leuven / Beerse / Schoten / Dendermonde / Overijse / Hooielaart / Mechelen / Breda /Eindhoven/Maastricht/Tilburg/Belgie/Nederlands / SSU / Study start-up / Submissions Specialist

Apply for this job: Study Start Up/Submission 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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