20 beste vacatures voor de functie van médical in zaventem, vlg (nieuwe medewerkers gezocht)

Experienced Clinical Research Associate, Multi-Sponsor, Belgium
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Thermo Fisher Scientific —Zaventem
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Toyota Motor Europe —Zaventem
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Regulatory Affairs Specialist
Hologic —Zaventem
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Oncology Emerging Therapeutics Medical Advisor
GlaxoSmithKline —Waver
- € 81.000 - € 135.000 per jaar
- Voltijds
- Doctoraat
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Chauffeur Bus - Autocar - permis D
Ciao365 —Zaventem
- € 18 - € 25 per uur
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- Engels
- Rijervaring
- Ter plaatse
Snel solliciteren
8 dagen
Quality Specialist
Hologic —Zaventem
- € 50.000 - € 70.000 per jaar
- ERP systemen
- Microsoft Office
- Bachelor
Regulatory and Start Up Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
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Study Start-up Associate II
ICON Plc —Mechelen
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
7 dagen
Study Start Up Management Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Bachelor
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Safety & Health Corporate Specialist
Toyota Motor Europe —Zaventem
- Microsoft Powerpoint
- Microsoft Excel
- Engels
BR Gazoo Racing (Senior) Specialist
Toyota Motor Europe —Zaventem
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12 dagen
Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA —Zaventem
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- Thuiswerk
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Safety & Health Corporate Ergo Specialist
Toyota Motor Europe —Zaventem
- Microsoft Powerpoint
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Field Medical Advisor Belgium - HAE & Immunoglobulins
CSL Behring —Mechelen
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Data Coordinator - CRO (Leuven, Entry-Level)
Medpace, Inc. —Leuven
- Voltijds
- Microsoft Word
- Microsoft Excel
- Bachelor
Clinical Quality and Compliance Manager
Cochlear Ltd —Mechelen
- Voltijds
- Verpleegkunde
- Engels
- Onderzoek

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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

médical vacatures in zaventem, vlg

Experienced Clinical Research Associate, Multi-Sponsor, Belgium

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Clinical Trials Assistant - Belgium, FSP

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Study Start Up Management Specialist - Belgium

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

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Field Medical Advisor Belgium - HAE & Immunoglobulins

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Clinical Quality and Compliance Manager

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van médical in zaventem, vlg

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