20 meilleures offres (regulatory specialist, brussels, bru) (à pourvoir)

Regulatory and Start Up Specialist - Belgium
IQVIA —Zaventem
- Temps plein
- Télétravail
- Expérience en supervision
- En présentiel
Regulatory Affairs Specialist
Hologic —Zaventem
- De 40 000 € à 50 000 € par an
- Microsoft Powerpoint
- Microsoft Word
- Espagnol
il y a 8 jours
Regulatory Affairs Officer
AbbVie —Wavre
- Temps plein
- Travail hybride
- Sens de l'organisation
- Compétences en communication
EHS Specialist
Medtronic —Bruxelles
- De 59 200 € à 88 800 € par an
- Temps partiel
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Specialist Customs Compliance EMEA
Ansell —Bruxelles
- Temps plein
- Travail hybride
- Systèmes PGI
- Esprit d'analyse
- Université
Regulatory Affairs Specialist
Nipro —Malines
- Bureau
- Esprit d'analyse
- Bachelier
Regulatory Affairs Specialist
Nipro Europe Group Companies —Malines
- Bureau
- Esprit d'analyse
- Bachelier
Operations Senior Specialist
ENTSO-E —Bruxelles
- Travail hybride
- Microsoft Excel
- Bureau
- Microsoft Office
Postuler rapidement
Medical Device UniQuality & Unidata Product Information Specialist
MSF International —Bruxelles
- Temps partiel
- Travail hybride
- Microsoft Excel
- Systèmes PGI
- Anglais
Postuler rapidement
Study Start Up Management Specialist - Belgium
IQVIA —Zaventem
- Temps plein
- Télétravail
- Recherche
- Bachelier
- En présentiel
il y a 12 jours
Global Trade and Tariffs Lead - 1 year contract starting in Sept/Oct 2026
Siemens Healthineers —City of Brussels
- Temps plein
- Travail hybride
- Anglais
Middle Office Oversight Officer F/M
CANDRIAM —Bruxelles
- Microsoft Excel
- Master
- Compétences en communication
Contract Law Associate
DIGI Belgium —Bruxelles
- De 3 000 € à 3 500 € par mois
- Temps plein
- Master
- En présentiel
- Compétences en communication
- Carte essence
- Remboursement des frais de téléphone
Postuler rapidement
Quality Specialist
Hologic —Zaventem
- De 50 000 € à 70 000 € par an
- Systèmes PGI
- Microsoft Office
- Bachelier
Business Development Manager, Competition/Antitrust, Regulation & Trade (CRT)
Herbert Smith Freehills —Bruxelles
- Temps plein
- Vente
- Master
- Développement commercial
AI Governance Specialist
Elia —Bruxelles
- Anglais
- Master
- Machine learning
il y a 13 jours
Operations Security Specialist
AXA —Bruxelles
- Informatique
- Informatique
- Anglais
Go To Market Manager for projects in Pharma & Life Sciences
PwC —Bruxelles
- Temps plein
- Travail hybride
- Vente
- Anglais
- Master
Regulatory Affairs - Environment
Nipro —Malines
- Travail hybride
- Bureau
- Master
- Bachelier
IT & Cyber Permanent Control Officer - HQ Brussels
BNP Paribas Fortis —Bruxelles
- Microsoft Powerpoint
- Microsoft Excel
- Master

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory specialist (brussels, bru)

En vous connectant à votre compte, vous acceptez les Conditions d'utilisation de SimplyHired et consentez à notre Politique relative aux cookies et Politique de confidentialité.

Afficher des offres d'emploi dans d'autres lieux

regulatory specialist jobs near brussels, bru

Regulatory and Start Up Specialist - Belgium

IQVIA -
Zaventem

Soumettre votre candidature

Détails de l'emploi

Temps plein

Qualifications

Français
Expérience en supervision

Description complète du poste

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.

Soumettre votre candidature

Affinez votre recherche

regulatory specialist emplois - brussels, bru

Regulatory and Start Up Specialist - Belgium

Regulatory Affairs Specialist

Regulatory Affairs Officer

EHS Specialist

Senior Specialist Customs Compliance EMEA

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Operations Senior Specialist

Medical Device UniQuality & Unidata Product Information Specialist

Study Start Up Management Specialist - Belgium

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

Middle Office Oversight Officer F/M

Contract Law Associate

Quality Specialist

Business Development Manager, Competition/Antitrust, Regulation & Trade (CRT)

AI Governance Specialist

Operations Security Specialist

Go To Market Manager for projects in Pharma & Life Sciences

Regulatory Affairs - Environment

IT & Cyber Permanent Control Officer - HQ Brussels

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory specialist (brussels, bru)

Related Searches

Afficher des offres d'emploi dans d'autres lieux

Where you'll work

Home-based

Culture

Outils pour les chercheurs d'emploi

Outils Employeurs

Parcourir

Garder le contact