i-Pharm Consulting

Pharmacovigilance (PV) Consultant (1FTE)

Location
Belgium
Salary
Negotiable
Posted
27 Nov 2018
Closes
11 Dec 2018
Ref
13724 - TJHB1
Contract Type
Contract
Pharmacovigilance (PV) Consultant, Belgium

An exciting CRO working on a variety of projects, requires a Pharmacovigilance (PV) Consultant. This role will include the opportunity of working with Medicinal Products and Medical Devices.

Job Title: Pharmacovigilance (PV) Consultant
Location: Belgium

Salary: Very Competitive hourly rate

Contract Length: 6-12 Months

1FTE

Contract position / Freelance position

Job Responsibilities:

* Provide Benelux support with Medical Devices and Active Pharmaceutical Ingredients (APIs)
* Act as Local Safety Officer
* Interacting with investigative sites based within the Benelux region
* Overseeing the submission of safety reports to the relevant Competent Authorities/Ethics Committees whilst complying with regulatory timelines.
* Monitor national pharmacovigilance regulations and notify relevant parties of any changes
* Train and mentor new hires.
* Benelux PV support therefore; No MeDra coding or EudraVigilance is required

Ideal Candidate:

* 4+ years of regulatory or comparable experience within a pharmaceutical company, CRO, or similar organization.
* Experience with both Medical Devices and Active Pharmaceutical Ingredients (APIs)
* Strong knowledge of regulatory requirements
* Fluency in French and Dutch
* No MeDra coding or EudraVigilance is required for this role.

To apply:
If you would like to discuss this vacancy further, please call Tom Jackman on +44 (0)20 3189 0490. 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:

www.i-pharmconsulting.com

Keywords:

Pharmacovigilance / Drug Safety / Pharma / PV /Drug Safety/ Clinical Safety / Clinical / PV Officer / Central Europe / Belgium / Brussels / Antwerp / Wavre / Charleroi

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