20 meilleures offres (quality specialist, puteaux, a8) (à pourvoir)

Country Associate Submissions Representative, France, IQVIA Biotech
IQVIA —Courbevoie (92)
- Temps plein
- Télétravail
- Niveau Licence
il y a 12 jours
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French Language Specialist (France) - Freelance AI Trainer Project
Meridial —Paris (75)
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- Master
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MRI Software Clinical Customer Success Manager/MTRA (France)
AIRS Medical Inc —Paris (75)
- De 70 000 € à 100 000 € par an
- Temps plein
- Télétravail
- Anglais
- Niveau Licence
- Compétences en communication
Postuler rapidement
Opérateur(trice) de saisie en laboratoire
Antech Diagnostics —Massy (91)
- Temps plein
- Expérience en cabinet médical
Gestionnaire administration des ventes (H/F)
Otis —Nanterre (92)
- Temps plein
- Microsoft Powerpoint
- Service client
- Niveau Bac +2
Bio Informatician,
GPI France —Paris (75)
- De 40 000 € à 45 000 € par an
- Temps plein
- Niveau Doctorat
- Anglais
- Master
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French Voice Actor - Freelance AI Trainer Project
Meridial —Paris (75)
- De 6 € à 65 € de l’heure
- Télétravail
Oliver Wyman - Recruiter - Experienced Hire - in Paris
Oliver Wyman —Paris (75)
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Consultant junior Data Analyst – Spécialiste data quality et data Gouvernance (F/H)
Deloitte —Puteaux (92)
- Ingénierie
- Anglais
- Master
Head of Talent Acquisition Manager (f/h/n)
Hublo —Paris (75)
- De 75 000 € à 90 000 € par an
- Télétravail partiel
- Anglais
- Gestion d'équipe
- Intelligence artificielle
Postuler rapidement
STEM Specialist (Fluent in French) - Freelance AI Trainer Project
Meridial —Paris (75)
- De 8 € à 65 € de l’heure
- Télétravail
- Informatique
- Master
- Machine learning
HRBP Director EU+APAC – Lab & Medical Operations
Antech Diagnostics —Massy (91)
- Temps plein
- Expérience en gestion d'équipe
- Master
Group Human Resources Controlling Senior Manager (M/F)
CMA CGM —Courbevoie (92)
- Microsoft Excel
- Anglais
- Master
CDD - Brand Marketing Manager (F/H/X)
Sephora —Neuilly-sur-Seine (92)
- Temps plein
- Microsoft Powerpoint
- Microsoft Excel
- Marketing
Account Health, Safety, Security & Environment Advisor
JLL —Paris (75)
- Négociation
Programme Specialist
UNESCO —Paris (75)
- 131 965 € par an
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- Niveau Doctorat
- Anglais
Specialist regulatory affairs and quality assurance for IVD medical devices
Advanced Biological Laboratories (ABL) —Paris (75)
- Anglais
Back Office Specialist
La Marzocco Group —Paris (75)
- Temps plein
- Microsoft Word
- Microsoft Excel
- Anglais
CDI - Brand Marketing Specialist (F/H/X)
Sephora —Neuilly-sur-Seine (92)
- Temps plein
- Microsoft Powerpoint
- Microsoft Excel
- Merchandising

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Country Associate Submissions Representative, France, IQVIA Biotech

IQVIA -
Courbevoie (92)

Soumettre votre candidature

Détails de l'emploi

Temps plein
Il y a 12 jours

Qualifications

Niveau Licence

Description complète du poste

Courbevoie, France | Full time | Home-based | R1563989

Country Associate Submissions Representative (Regulatory & Start-Up Specialist)

Homebased

France

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.

Job Summary

The Site Activation Specialist is responsible for coordinating and executing site start-up and activation activities for clinical research studies in accordance with applicable regulations, SOPs, project requirements, and timelines. The role serves as a key point of contact for investigative sites and project teams, ensuring the timely preparation, review, and tracking of regulatory and essential study documents.

Key Responsibilities

Act as the primary contact for assigned investigative sites and project stakeholders during site activation activities.
Perform site start-up and activation activities in compliance with applicable regulations, SOPs, and work instructions.
Prepare, review, and maintain site regulatory documentation, ensuring accuracy and completeness.
Track approvals and execution of regulatory, ethics, informed consent, and study-related documents to meet project timelines.
Maintain project information in internal systems, databases, and tracking tools.
Monitor site performance metrics and provide updates to management and project teams.
Support project planning, timeline management, and implementation of contingency plans when required.
Perform quality control reviews of site documentation.
Provide local regulatory and site activation expertise to project teams and stakeholders.

Qualifications

Bachelor's degree in Life Sciences, Health Sciences, or a related field.
Minimum 1 year of clinical research experience.
Knowledge of contract amendments and updating of ICFs beneficial.
Knowledge of clinical research regulations, Good Clinical Practice (GCP), and site activation processes.
Strong organizational, communication, and relationship management skills.
Ability to manage multiple priorities and meet project deadlines.

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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quality specialist emplois - puteaux, a8

Country Associate Submissions Representative, France, IQVIA Biotech

Gestionnaire de contrat clients France-Belgique f/h/nb

French Language Specialist (France) - Freelance AI Trainer Project

MRI Software Clinical Customer Success Manager/MTRA (France)

Opérateur(trice) de saisie en laboratoire

Gestionnaire administration des ventes (H/F)

Bio Informatician,

French Voice Actor - Freelance AI Trainer Project

Oliver Wyman - Recruiter - Experienced Hire - in Paris

Consultant junior Data Analyst – Spécialiste data quality et data Gouvernance (F/H)

Head of Talent Acquisition Manager (f/h/n)

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

HRBP Director EU+APAC – Lab & Medical Operations

Group Human Resources Controlling Senior Manager (M/F)

CDD - Brand Marketing Manager (F/H/X)

Account Health, Safety, Security & Environment Advisor

Programme Specialist

Specialist regulatory affairs and quality assurance for IVD medical devices

Back Office Specialist

CDI - Brand Marketing Specialist (F/H/X)

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : quality specialist (puteaux, a8)

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Where you'll work

Home-based

Culture

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