20 beste vacatures voor de functie van associate, ehs operations, pds emea in brussels, bru (nieuwe medewerkers gezocht)

Experienced Clinical Research Associate, Multi-Sponsor, Belgium
IQVIA —Zaventem
- Voltijds
- Onderzoek
- Microsoft Office
- Master
Associate, EHS Operations, PDS EMEA
Cushman & Wakefield —Brussel
- Engels
- Bouw
- Ter plaatse
Snel solliciteren
EHS Specialist
Medtronic —Brussel
- € 59.200 - € 88.800 per jaar
- Deeltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Consultant Research & Development in Pharma & Life Sciences
PwC —Brussel
- Voltijds
- Hybride werken
- Microsoft Powerpoint
- Microsoft Excel
- Onderzoek
Support Laboratoire Polyvalent
Avantor —Eigenbrakel
- Voltijds
- Microsoft Excel
- Engels
- Microsoft Office
OTC, MD & IP Support Analyst EMEA
Terumo —Leuven
- Microsoft Excel
- Salesforce
- ERP systemen
Site Management Associate I
PSI CRO —Leuven
- Voltijds
- Hybride werken
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Snel solliciteren
Junior Associate (October 2026) (Ref. : 2025-1261) - Junior Associate
KPMG —Zaventem
- Voltijds
- Schrijfvaardigheden
- Geen ervaring nodig
- Engels
Clinical Trials Assistant - Belgium, FSP
IQVIA —Zaventem
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Lab Supply Operations Specialist
Avantor —Eigenbrakel
- Voltijds
- Microsoft Excel
- Engels
- Microsoft Office
Investigation & Process Improvement Coordinator
GlaxoSmithKline —Waver
- € 53.625 - € 89.375 per jaar
- Voltijds
- Organisatorische vaardigheden
8 dagen
Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Master
- Managementervaring
Technical Support Representative
Hologic —Zaventem
- € 55.000 - € 65.000 per jaar
- Spaans
- Klantenservice
- Salesforce
Associate Analyst, Strategy & Business Excellence – Europe (Rosetta Contract)
Mastercard —Waterloo
- Voltijds
- Microsoft Powerpoint
- Microsoft Excel
- Engels
Associate - Operations
Wesco —Antwerpen
- Voltijds
- Geen ervaring nodig
- Secundair Onderwijs
Junior Project Management Officer (PMO) | Nuclear Energy
Capgemini Sogeti —Diegem
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Junior Project Management Officer (PMO) | Nuclear Energy
Capgemini —Diegem
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research associate in Purification (M/F)
Novalix —Eigenbrakel
- Master
- Bachelor
5 dagen
Supervisor II, Onsite Lab Operations Support
Avantor —Eigenbrakel
- Voltijds
- Microsoft Excel
- Microsoft Outlook
- Management
Junior Data Analytics Consultant - 2026
PwC —Brussel
- Voltijds
- Hybride werken
- Azure
- Master
- SQL

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Experienced Clinical Research Associate, Multi-Sponsor, Belgium

IQVIA -
Zaventem

Nu solliciteren

Vacaturegegevens

Voltijds

Extralegale voordelen

Bedrijfswagen

Kwalificaties

Frans
Onderzoek
Microsoft Office
Master
Computervaardigheden
Tijdsbeheer

Volledige vacaturetekst

Zaventem, Belgium | Full time | Office-based | R1552876

Clinical Research Associate

IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Your responsibilities will include:

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Your Profile

University degree in scientific discipline or health care
2+ years of experience as a CRA
Very good computer skills including MS Office
Excellent command of Dutch, French and English language. Belgium based.
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility to travel
Driver’s license class B

What you can expect:

Resources that promote your career growth
Leaders that support flexible work schedules
Programs to help you build your therapeutic knowledge
Excellent working environment in a stabile, international, reputable company
Company car, mobile phone and attractive benefits packaging

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

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

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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Verfijn je zoekopdracht

associate, ehs operations, pds emea vacatures in brussels, bru

Experienced Clinical Research Associate, Multi-Sponsor, Belgium

Associate, EHS Operations, PDS EMEA

EHS Specialist

Consultant Research & Development in Pharma & Life Sciences

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Site Management Associate I

Junior Associate (October 2026) (Ref. : 2025-1261) - Junior Associate

Clinical Trials Assistant - Belgium, FSP

Lab Supply Operations Specialist

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Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)

Technical Support Representative

Associate Analyst, Strategy & Business Excellence – Europe (Rosetta Contract)

Associate - Operations

Junior Project Management Officer (PMO) | Nuclear Energy

Junior Project Management Officer (PMO) | Nuclear Energy

Research associate in Purification (M/F)

Supervisor II, Onsite Lab Operations Support

Junior Data Analytics Consultant - 2026

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van associate, ehs operations, pds emea in brussels, bru

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