i-Pharm Consulting

Regulatory Affairs Officer

07 Jan 2019
21 Jan 2019
Contract Type
Regulatory Affairs Officer, Belgium

An exciting opportunity has arisen to join a leading CRO and manage their regulatory activities. You will be involved in a wide variety of exciting projects and clinical trials.

Job Title: Regulatory Affairs Officer
Location: Belgium

Benefits: Above market rate salary + fantastic benefits package

Permanent position

Job Responsibilities:

* Prepare clinical trial submission dossiers
* Coordinate Belgium regulatory responsibilities and support the central regulatory teams
* Provide support for new product submissions
* Review translations of essential documents
* Manage safety reporting to relevant authorities

Ideal Candidate:

* Experience of Clinical Trial submissions within Belgium
* Good communication, interpersonal interaction and organisational skills are essential
* Life sciences degree or equivalent qualification and training
* Working proficiency in Dutch, French and English

To apply:
If you would like to discuss this vacancy further, please call Tom Jackman on +44 (0)20 3189 0490, or email tjackman@i-pharmconsulting.com. If this role is not suitable, Tom is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

About i-Pharm

i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm Regulatory is a team within the larger organisation i-Pharm Consulting which provides candidates in areas such as: Clinical Operations, Pharmacovigilance, Biometrics, Project Managements, Quality Assurance and Health Economics. Visit our website to see our extensive current vacancies:



Regulatory Affairs / Reg Affairs / RA / Regulatory Affairs Officer / Reg Affairs Officer / RA Officer / systems / variations / dossier / labelling / registrations / renewals / submissions / CMC / Central Europe / Belgium / Brussels / Antwerp / Wavre / Charleroi / Leuven

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