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

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Transfer Pricing (Senior) Manager
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Consultant Learning Experience
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Manager M&A Transaction Services
Deloitte —Zaventem
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Internal Audit Manager, Fincrime
Wise Australia Investments —Brussel
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Director M&A Transaction Services
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Hospital Representative/ Product Specialist
Alfasigma Group —Mechelen
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M&A Data Analytics Manager
Deloitte —Zaventem
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HR Professional
Siemens Healthineers —Dilbeek
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Omp Implementation Senior Consultant (Supply Chain Planning)
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Senior Technology Product Specialist – Rewards Technology
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HR Specialist (Fluent in French) - Freelance AI Trainer Project
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Head of Market Access BeNeLux
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People Relations Specialist, Sales Market Benelux – Belgium & Luxembourg (m/f/d)
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Go To Market Manager for projects in Pharma & Life Sciences
PwC —Brussel
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Key Account Manager Wallonia
Carrier —Zaventem
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4 dagen

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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

global health specialist vacatures in zaventem, vlg

Study Start Up Management Specialist - Belgium

Safety & Health Corporate Specialist

Safety & Health Corporate Ergo Specialist

Regulatory and Start Up Specialist - Belgium

Senior Payroll Specialist

Transfer Pricing (Senior) Manager

Consultant Learning Experience

Manager M&A Transaction Services

Internal Audit Manager, Fincrime

Director M&A Transaction Services

Hospital Representative/ Product Specialist

M&A Data Analytics Manager

HR Professional

Omp Implementation Senior Consultant (Supply Chain Planning)

Senior Technology Product Specialist – Rewards Technology

HR Specialist (Fluent in French) - Freelance AI Trainer Project

Head of Market Access BeNeLux

People Relations Specialist, Sales Market Benelux – Belgium & Luxembourg (m/f/d)

Go To Market Manager for projects in Pharma & Life Sciences

Key Account Manager Wallonia

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van global health specialist in zaventem, vlg

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