14 meilleures offres (total safety, antwerpen (provincie)) (à pourvoir)

Clinical Site Manager II
ICON Plc —Malines
- Temps plein
- Recherche
- Soins infirmiers
Clinical Project Associate Belgium
サイネオス・ヘルス —Anvers (province)
- Recherche
- Master
Asset Life Cycle Lead
Novartis —Puurs
- De 61 300 € à 113 900 € par an
- Temps plein
- Master
- Gestion de projet
- Bachelier
- Assurance groupe
il y a 10 jours
Operations Manager Olen | Plukon Food Group
VALPEO —Kempen
- Esprit d'analyse
- Production
- Intelligence artificielle
Postuler rapidement
CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab Inc. —Berchem
- Temps plein
- Doctorat
- Vente
- Anglais
il y a 3 jours
Process Engineer
Mondelēz International —Herentals
- Microsoft Excel
- Anglais
- Windows
Lead CRA (Sponsor dedicated) Belgium
サイネオス・ヘルス —Anvers (province)
- Recherche
- Bachelier
Process Engineer Plastics
Greif —Lierre
- De 49 900 € à 84 900 € par an
- Temps plein
Food & Beverage Sales Area Manager – Supply Chain Assurance services
DNV —Anvers
- Temps plein
- Vente
- Anglais
- Recherche
CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab —Berchem
- Temps plein
- Doctorat
- Vente
- Anglais
il y a 3 jours
Business Development Manager Professional Scientific Services Belgium
Eurofins —Malines
- Temps plein
- Travail hybride
- Master
- Développement commercial
- Production
- Carte essence
Postuler rapidement
Senior Project Manager - Electrical
Equans —Anvers
- Temps plein
- Expérience en gestion d'équipe
- Chantier
- Construction et rénovation
Accounting Manager
Kemin —Herentals
- Temps plein
- Systèmes PGI
- Anglais
- Bachelier
Operator Staal
Greif —Lierre
- Temps plein
- Anglais

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Clinical Project Associate Belgium
サイネオス・ヘルス —Anvers (province)
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and…

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Clinical Site Manager II

ICON Plc -
Malines

Soumettre votre candidature

Détails de l'emploi

Temps plein

Qualifications

Recherche
Collecte de données
Soins infirmiers

Description complète du poste

Snr CRA I Clinical Site Manager

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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

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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total safety emplois - antwerpen (provincie)

Clinical Site Manager II

Clinical Project Associate Belgium

Asset Life Cycle Lead

Operations Manager Olen | Plukon Food Group

CMC Biopharma Regulatory Consultant — Ecolab Life Sciences

Process Engineer

Lead CRA (Sponsor dedicated) Belgium

Process Engineer Plastics

Food & Beverage Sales Area Manager – Supply Chain Assurance services

CMC Biopharma Regulatory Consultant — Ecolab Life Sciences

Business Development Manager Professional Scientific Services Belgium

Senior Project Manager - Electrical

Accounting Manager

Operator Staal

More jobs to discover

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