i-Pharm Consulting

Site Activation Specialist - Belgium (CRO)

Location
Belgium
Salary
Negotiable
Posted
15 Nov 2018
Closes
13 Feb 2019
Ref
SASB78549
Contract Type
Permanent
SITE ACTIVATION SPECIALIST | BELGIUM | GLOBAL CRO



Are you looking for a new working environment, with a flexible employer that will boost your progression? A Global CRO are looking for a Site Activation Specialist to join their team in the Belgium. The client have a pipeline of upcoming ground breaking global studies within a range of therapeutic fields. They are currently looking for someone to perform these duties for global trials. The company are offering fantastic opportunities to work reduced hours and to work more hours at home to avoid traffic. Added to this there is a fantastic salary package with this job offer, read on to find out more!



JOB TITLE



Site Activation Specialist



LOCATION

Belgium



SALARY & BENEFITS

Very Competitive Salary package + Benefits

+13th month

+Reimbursement of Mileage/Transportation allowance

+Pension

+Healthcare

+Life insurance

+Meal vouchers

+Phone

+Laptop

+Flexibility to work from home



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. You will also be in charge of negotation of contracts, costumaization

of ICF and more. The would be candidate 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

Study activation experience of at least 12 months

Life Sciences Degree or equivalent, in a scientific or healthcare discipline

Vast knowledge of the local requirements for submissions

Experience working in a CRO or Pharma Company

Must speak French, Dutch and English (flexible for fluency)





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 Clinical Operations Consultant Mak Ishola on +32 (0)2 808 2151, 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

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