20 beste vacatures voor de functie van regulatory specialist in zaventem (nieuwe medewerkers gezocht)

Regulatory and Start Up Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Leidinggevende ervaring
- Ter plaatse
Regulatory Affairs Specialist
Hologic —Zaventem
- € 40.000 - € 50.000 per jaar
- Microsoft Powerpoint
- Microsoft Word
- Spaans
8 dagen
EHS Specialist
Medtronic —Brussel
- € 59.200 - € 88.800 per jaar
- Deeltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Specialist Customs Compliance EMEA
Ansell —Brussel
- Voltijds
- Hybride werken
- ERP systemen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Officer
AbbVie —Waver
- Voltijds
- Hybride werken
- Organisatorische vaardigheden
- Communicatieve vaardigheden
HR International Mobility Officer
Daikin Europe N.V. —Brussel
- Microsoft Excel
- Engels
- Microsoft Office
Operations Senior Specialist
ENTSO-E —Brussel
- Hybride werken
- Microsoft Excel
- Microsoft Office
- Master
Snel solliciteren
Global Trade and Tariffs Lead - 1 year contract starting in Sept/Oct 2026
Siemens Healthineers —City of Brussels
- Voltijds
- Hybride werken
- Engels
Medical Device UniQuality & Unidata Product Information Specialist
MSF International —Brussel
- Deeltijds
- Hybride werken
- Microsoft Excel
- ERP systemen
- Engels
Snel solliciteren
Finance And Accounting Consultant (Outsourcing)
Deloitte —Zaventem
- Deeltijds
- ERP systemen
- Microsoft Office
- Master
Quality Specialist
Hologic —Zaventem
- € 50.000 - € 70.000 per jaar
- ERP systemen
- Microsoft Office
- Bachelor
Indirect Tax Transformation Consultant (Ref. : 2025-1281) - Senior Tax Adviser
KPMG —Zaventem
- Voltijds
- ERP systemen
Cloud Infrastructure Specialist (Ref. : 2026-1395) - Senior Advisor
KPMG —Zaventem
- Voltijds
- Azure
- ERP systemen
- Master
- Thuiswerkopties
Process Expert (M/F)
SUEZ —Brussel
- Engels
- Master
- Analytisch vermogen
Senior Consultant/Manager IT Controls & Governance and IT Assurance
Deloitte —Zaventem
- Deeltijds
- Microsoft Powerpoint
- Microsoft Excel
- Projectmanagement
Contract Law Associate
DIGI Belgium —Brussel
- € 3.000 - € 3.500 per maand
- Voltijds
- Master
- Ter plaatse
- Communicatieve vaardigheden
- Tankkaart
- GSM-vergoeding
Snel solliciteren
Clinical Supply Compliance Governance Lead
UCB —Eigenbrakel
- Engels
- Master
- Bachelor
11 dagen
Study Start Up Management Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Bachelor
- Ter plaatse
12 dagen

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Regulatory and Start Up Specialist - Belgium

IQVIA -
Zaventem

Nu solliciteren

Vacaturegegevens

Voltijds

Kwalificaties

Frans
Leidinggevende ervaring

Volledige vacaturetekst

Zaventem, Belgium | Full time | Home-based | R1547016

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Home Based role - requiring Dutch / French language fluency and local submissions as well as contract negotiations experience.

Essential Functions
Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.

Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.

Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines.

Ensure monitoring measures are in place and implement contingency plan as needed.

Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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regulatory specialist vacatures in zaventem

Regulatory and Start Up Specialist - Belgium

Regulatory Affairs Specialist

EHS Specialist

Senior Specialist Customs Compliance EMEA

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Regulatory Affairs Officer

HR International Mobility Officer

Operations Senior Specialist

Global Trade and Tariffs Lead - 1 year contract starting in Sept/Oct 2026

Medical Device UniQuality & Unidata Product Information Specialist

Finance And Accounting Consultant (Outsourcing)

Quality Specialist

Indirect Tax Transformation Consultant (Ref. : 2025-1281) - Senior Tax Adviser

Cloud Infrastructure Specialist (Ref. : 2026-1395) - Senior Advisor

Process Expert (M/F)

Senior Consultant/Manager IT Controls & Governance and IT Assurance

Contract Law Associate

Clinical Supply Compliance Governance Lead

Study Start Up Management Specialist - Belgium

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory specialist in zaventem

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