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Job Details

Global Clinical Submissions Specialist

Company: i-Pharm Consulting
Location: Belgium
Reference: GCSS2000
Closing Date: 28 May 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

GLOBAL CLINICAL SUBMISSIONS SPECIALIST | BELGIUM | TOP 10 GLOBAL PHARMACEUTICAL COMPANY A global pharma company is looking for a Submission Specialist to join their departement in Belgium. This international company 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. Would be candidate must have extensive experience in study start up processes as well as regulatory and EC submissions. ...

Requirements:

GLOBAL CLINICAL SUBMISSIONS SPECIALIST | BELGIUM | TOP 10 GLOBAL PHARMACEUTICAL COMPANY



A global pharma company is looking for a Submission Specialist to join their departement in Belgium. This international company 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. Would be candidate must have extensive experience in study start up processes as well as regulatory and EC submissions.



JOB TITLE

Global Clinical Submissions Specialist



LOCATION

Belgium



SALARY & BENEFITS

Up to 65,000€ per annum salary + Secondary benefits

+13th month

+Pension plan

+Healthcare

+Life insurance

+Meal vouchers



ROLE/DESCRIPTION

In charge of different regulatory submissions as well as the preparation and review of global ethics.

To work directly with global regulatory authorities.

Will be the key person on the global 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/or English (English and one local language is sufficient)





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

Study Start up Specialist/ Country Approval Specialist / Site Initiation associate / Site Initiation Specialist / Site Start Up Specialist / Initiation Associate / Initiation Speciailist / 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: Global Clinical 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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