Submissions Specialist - Netherlands

SUBMISSIONS SPECIALIST | THE NETHERLANDS | PERMANENT CONTRACT

A company involved in pharmaceutical research in the Netherlands are looking for a Study Start-up Associate to join their team. This international company is one of the industry and in the whole market and is looking for ambitious candidates who are willing to join for a new challenge for their career. Applicants must speak English and Dutch fluently and have submissions experience in the Netherlands.

JOB TITLE

Submissions Specialist

LOCATION

The Netherlands

SALARY & BENEFITS

Very Competitive Salary package + Benefits

+13th month

+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. You will work closely with the CRA's and CPM's for site activation processes. You will work directly with local regulatory authorities and 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

Site activation experience of over a year (more experienced candidates are also sough after)

Regulatory experience and/or submissions experience

Strong knowledge of medical terminology knowledge

Experience working in a CRO or Pharma Company would be a plus

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 the Benelux Consultant Mak Ishola on +31 2 808 1497 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 / Site Initiation associate / Site Initiation Specialist / Site Start Up Specialist / Initiation Associate / Site Activation Specialist / Initiation Specialist / CRA / CTA / CRAI / CRA II / SSU / Senior CRA / SCRA / Submission Specialist / Senior Research Monitor/ Senior Clinical Trial Monitor / Senior Clinical Site Manager / Senior CSM / CSM / Clinical Site Manager / CRA / CRAI / CRA II / SSU / Senior CRA / SCRA / Senior Clinical Research / 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 / 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/ ICH-GCP / Clinical Research /Central Europe / Regulatory Affairs / Regulatory Documents / ICH-GCP / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Office -Based / Amsterdam / Rotterdam / Utrecht / Eindhoven / Den Haag / Nijmegen / Lent / Rotterdam / Arnhem / Breda / Maastricht / Tilburg /Groningen / Holland / Noord Holland /Zuid Holland / Noord Brabant / Nederland