20 meilleures offres (project lead, antwerpen) (à pourvoir)

Regulatory Liaison
ICON Plc —Malines
- Temps plein
- Bachelier
il y a 2 jours
Project Procurement Lead
INEOS Group —Anvers
- De 101 181 € à 153 234 € par an
- Temps plein
- Anglais
- Microsoft Office
- Master
12 h
Project Procurement Lead
INEOS —Anvers
- De 101 181 € à 153 234 € par an
- Temps plein
- Anglais
- Microsoft Office
- Master
Postuler rapidement
il y a 1 jour
Project Lead
Tech-Solutions —Anvers
- Master
- Compétences en communication
Connectivity and Data Project Lead
Atlas Copco Group —Anvers
- Anglais
- Master
- Gestion de projet
il y a 1 jour
Project Lead Merchandising
Smollan Belgium —Anvers
- Merchandising
- Sens de l'organisation
- Travail à domicile
Postuler rapidement
Project Control Lead
Benton —Anvers
- Microsoft Excel
- Anglais
- Master
- Carte essence
il y a 12 jours
Project Manager
Cyclops —Malines
- Travail hybride
- Leadership
- Carte essence
Senior Project Manager
KION Group AG —Anvers
- Temps plein
- Gestion de projet
- Compétences en communication
Technical Procurement Lead
INEOS Group —Anvers
- De 101 181 € à 175 027 € par an
- Temps plein
- Expérience en gestion d'équipe
- Microsoft Office
- Master
12 h
Project Buyer
GEA Group Aktiengesellschaft —Wommelgem
- Temps plein
- Systèmes PGI
- Master
- Gestion de projet
il y a 14 jours
Medior Project Manager
Cyclops —Malines
- Travail hybride
- Anglais
- Master
- Bachelier
Assay Development Scientist - Genomics Services (Hybrid)
CellCarta —Wilrijk
- Temps plein
- Travail hybride
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Technical Procurement Lead
INEOS —Anvers
- De 101 181 € à 175 027 € par an
- Temps plein
- Expérience en gestion d'équipe
- Microsoft Office
- Master
Postuler rapidement
il y a 1 jour
Project Manager (m/f/d)
Orise GmbH —Anvers
- Anglais
- Gestion de projet
- Compétences en communication
Assistant Project Manager Electricity
Imtech —Wommelgem
- Chantier
- Anglais
- Esprit d'analyse
Business Project Specialist
BMW —Aartselaar
- Microsoft Office
- Master
- Bachelier
(Student) Community Manager
Specter —Anvers
- Temps partiel
- Logiciels de GRC/CRM
- Vente
- Systèmes PGI
Postuler rapidement
Head Of Onboarding
Rydoo —Anvers
- Temps plein
- Travail hybride
- Systèmes PGI
- Anglais
- Master
Postuler rapidement
Project Lead
Stroohm —Schelle
- Temps plein
- Gestion de projet
- Bachelier
il y a 9 jours

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Regulatory Liaison

ICON Plc -
Malines

Soumettre votre candidature

Détails de l'emploi

Temps plein
Il y a 2 jours

Qualifications

Bachelier

Description complète du poste

Regulatory Liaison

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Regulatory liaison to join our diverse and dynamic team. The Regulatory liaison will act as the primary regulatory interface for clinical trial teams, ensuring compliance with global and local regulations, facilitating timely submissions, and maintaining transparency throughout the trial lifecycle. This role bridges regulatory strategy and operational execution, supporting CTR Excellence objectives

This role is fully embedded with a hugely innovative Biotech where pioneering scientists and antibody engineers work side-by-side to accelerate the discovery of novel targets, disease pathways and differentiated therapeutic antibodies within Immunology.

What you will do:

Represent Regulatory Affairs at Clinical Trial Teams (CTTs) and cross-functional meetings.
Serve as the main point of contact for clinical trials regulatory matters between argenx and partners.
Prepare, review, and coordinate regulatory submission packages (CTAs, amendments, IBs, IMPDs) with partners.
Ensure timely and accurate submissions in compliance with EU CTR, and other regional requirements.
Monitor delegated activities and maintain oversight of regulatory deliverables.
Ensure adherence to global and local regulatory standards and company SOPs.
Liaise with Transparency Lead/Liaisons to ensure compliance with disclosure requirements.
Maintain accurate documentation and tracking of regulatory activities.
Contribute to process improvements and best practices within CTR Excellence.
Collaborate closely with Regulatory Scientists, Regulatory Coordinators and External Partners to optimize workload.

You will have:

Regulatory Expertise: Strong knowledge of EU Clinical Trial Regulation (CTR) and global regulatory frameworks.
Project Management:
Ability to manage complex tasks, prioritize effectively, and meet tight timelines.
Attention to detail.
Effectively and proactively collaborates per operating principles to drive assignments.
Ability to interpret regulatory guidelines and apply them to operational processes.
Problem-solving mindset: sound judgement and ability to analyse situations and information. Takes decisions based on facts and figures rather than on assumptions

Your Profile:

You will bring relevant regulatory affairs experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Strong Regulatory submission and EU CTR experience essential
Experience in cross-functional teams

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : project lead (antwerpen)

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