20 beste vacatures voor de functie van clinical project in duffel (nieuwe medewerkers gezocht)

Study Start Up Management Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Bachelor
- Ter plaatse
Clinical Project Manager
Deltaclinical —Willebroek
- Deeltijds
- Hôpital
- Engels
Assay Development Scientist - Genomics Services (Hybrid)
CellCarta —Wilrijk
- Voltijds
- Hybride werken
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4 dagen
Bioinformatics Scientist - Genomics Services
CellCarta —Wilrijk
- Voltijds
- Azure
- Master
- AWS
Clinical Study Specialist I
CellCarta —Wilrijk
- Voltijds
- Onderzoek
- Master
- Ter plaatse
2 dagen
Service Engineer Global Services & Support Imaging SLS BBIO Group (m/f/d)
Bruker —Kontich
- Thuiswerk
- ERP systemen
- Engels
- Microsoft Office
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Projectmanagement
- Bachelor
Clinical Research Associate, Multi-Sponsor, Belgium
IQVIA —Zaventem
- Voltijds
- Microsoft Office
- Master
- Computervaardigheden
Regulatory and Start Up Specialist - Belgium
IQVIA —Berchem
- Voltijds
- Thuiswerk
- Leidinggevende ervaring
- Ter plaatse
Clin Ops Manager
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
11 dagen
Clinical Research Associate - French Speaking - Any EMEA location
North American Science Associates Ltd. —Antwerpen
- Onderzoek
- Master
- Organisatorische vaardigheden
Snel solliciteren
Junior Consultant - Pharma
IQVIA —Kampenhout
- Voltijds
- Master
- Communicatieve vaardigheden
Medical and Clinical Affairs Director
Flen Health GmbH —Kontich
- Doctoraat
- Verkoopervaring
- Bedrijfsontwikkeling
Post-doctoral Scientist Vaccine Immunogenicity (Ebola Outbreak Response)
Instituut voor Tropische Geneeskunde —Antwerpen
- € 6.416,44 per maand
- Voltijds
- Doctoraat
- Engels
- Analytisch vermogen
7 dagen
Clinical Forecasting Specialist - Sponsor Dedicated
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Microsoft Excel
- Bachelor
- Accountancy
(Senior) Manager Logistics Consulting – Life Science
Bluecrux —Mechelen
- Voltijds
- Hybride werken
- ERP systemen
- Master
Snel solliciteren
Senior Quality Engineer - Qualified Person
Labcorp —Mechelen
- Voltijds
- Engels
- Onderzoek
- Master
Principal, Health Economics, Health Technology Assessment
IQVIA —Antwerpen
- Voltijds
- Microsoft Excel
- Master
- ICT
Senior Manager, Facilities and EH&S
CellCarta —Wilrijk
- Voltijds
- AutoCAD
- HVAC
- Bouw
11 dagen
Professor of Child and Adolescent Health
Instituut voor Tropische Geneeskunde —Antwerpen
- Doctoraat
- Onderzoek
- Verhuiskostenvergoeding

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical project in duffel

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Study Start Up Management Specialist - Belgium

IQVIA -
Zaventem

Nu solliciteren

Vacaturegegevens

Voltijds

Kwalificaties

Frans
Onderzoek
Bachelor

Volledige vacaturetekst

Zaventem, Belgium | Full time | Home-based | R1558265

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Home Based role requiring local submissions experience as well as fluency within Dutch, French and English.

Essential Functions

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.
Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines.
Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience.

Ability to manage multiple projects.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.

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

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

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

clinical project vacatures in duffel

Study Start Up Management Specialist - Belgium

Clinical Project Manager

Assay Development Scientist - Genomics Services (Hybrid)

Bioinformatics Scientist - Genomics Services

Clinical Study Specialist I

Service Engineer Global Services & Support Imaging SLS BBIO Group (m/f/d)

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

Clinical Research Associate, Multi-Sponsor, Belgium

Regulatory and Start Up Specialist - Belgium

Clin Ops Manager

Clinical Research Associate - French Speaking - Any EMEA location

Junior Consultant - Pharma

Medical and Clinical Affairs Director

Post-doctoral Scientist Vaccine Immunogenicity (Ebola Outbreak Response)

Clinical Forecasting Specialist - Sponsor Dedicated

(Senior) Manager Logistics Consulting – Life Science

Senior Quality Engineer - Qualified Person

Principal, Health Economics, Health Technology Assessment

Senior Manager, Facilities and EH&S

Professor of Child and Adolescent Health

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical project in duffel

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