20 beste vacatures voor de functie van clinical trial in belgium (nieuwe medewerkers gezocht)

Clinical Research Associate, Multi-Sponsor, Belgium
IQVIA —Zaventem
- Voltijds
- Microsoft Office
- Master
- Computervaardigheden
Clinical Project Associate Belgium
サイネオス・ヘルス —Antwerpen (provincie)
- Onderzoek
- Master
Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Master
- Managementervaring
Medical Technologist I
Thermo Fisher Scientific —Zaventem
- Weekendbeschikbaarheid
- Microsoft Office
- Bachelor
- Organisatorische vaardigheden
Junior Medical Writer
Emtex —Sint-Gillis-Waas
- Voltijds
- Thuiswerk
- Schrijfvaardigheden
- Master
- Computervaardigheden
Oncology Emerging Therapeutics Medical Advisor
GlaxoSmithKline —Waver
- € 81.000 - € 135.000 per jaar
- Voltijds
- Doctoraat
- Onderzoek
- Artificiële intelligentie
Clinical Quality and Compliance Manager
Cochlear Ltd —Mechelen
- Voltijds
- Verpleegkunde
- Engels
- Onderzoek
Senior/ Medical Writer - FSP
IQVIA —Zaventem
- Voltijds
- Microsoft Word
- Doctoraat
- Onderzoek
10 dagen
Bioinformatics Scientist - Genomics Services
CellCarta —Wilrijk
- Voltijds
- Azure
- Master
- AWS
Clinical Research Associate (Belgium, Netherlands)
Allucent —Scherpenheuvel
- Hybride werken
Snel solliciteren
Clinical Research Consultant (CRC)
KasaConsult —Hoegaarden
Site Enrollment and Engagement Lead
IQVIA —Berchem
- Voltijds
- Thuiswerk
- Engels
- Onderzoek
- Bachelor
Principal Medical Writer (Publications)
Thermo Fisher Scientific —Werk van thuis
- Voltijds
- Thuiswerk
- Analytisch vermogen
- Bachelor
Study Start-up Associate II
ICON Plc —Mechelen
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12 dagen
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Projectmanagement
- Bachelor
9 dagen
Program Manager, Regulatory Medical Writing - Client-dedicated FSP
Thermo Fisher Scientific —Werk van thuis
- Voltijds
- Thuiswerk
- Bachelor
- Onderhandelen
Regulatory Affairs Associate (80/100%)
KasaConsult —Hoegaarden
- Microsoft Office
Clinical Site Manager II
ICON Plc —Mechelen
- Voltijds
- Onderzoek
- Verpleegkunde
Enterprise Account Executive – Healthcare Logistics & Freight Forwarding
UPS —Machelen
- € 4.900 per maand
- Voltijds
- Bachelor
- Onderhandelen
Legal Counsel, Clinical Development
Argenx —Gent
- Voltijds
- Engels
- Analytisch vermogen
- Projectmanagement
12 dagen

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Clinical Research Associate, Multi-Sponsor, Belgium

IQVIA -
Zaventem

Nu solliciteren

Vacaturegegevens

Voltijds

Extralegale voordelen

Bedrijfswagen

Kwalificaties

Frans
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 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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clinical trial vacatures in belgium

Clinical Research Associate, Multi-Sponsor, Belgium

Clinical Project Associate Belgium

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

Medical Technologist I

Junior Medical Writer

Oncology Emerging Therapeutics Medical Advisor

Clinical Quality and Compliance Manager

Senior/ Medical Writer - FSP

Bioinformatics Scientist - Genomics Services

Clinical Research Associate (Belgium, Netherlands)

Clinical Research Consultant (CRC)

Site Enrollment and Engagement Lead

Principal Medical Writer (Publications)

Study Start-up Associate II

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Program Manager, Regulatory Medical Writing - Client-dedicated FSP

Regulatory Affairs Associate (80/100%)

Clinical Site Manager II

Enterprise Account Executive – Healthcare Logistics & Freight Forwarding

Legal Counsel, Clinical Development

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical trial in belgium

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