20 meilleures offres (clinical data manager, france) (à pourvoir)

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- Temps plein
- Anglais
- Leadership
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- Microsoft Powerpoint
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- Niveau Licence
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- Master
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Implicity —Paris (75)
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- Niveau Doctorat
- Anglais
- Master
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Fortrea —Paris (75)
- Temps plein
- Anglais
- Soins infirmiers
il y a 11 jours
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CHRU de Brest —Brest (29)
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- Compétences rédactionnelles
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- SQL
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DATA MANAGER (H/F)
Hôpital Morvan —Brest (29)
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- Compétences rédactionnelles
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Clinical Trial Manager - Sponsor dedicated - Based in Rueil Malmaison
サイネオス・ヘルス —Montrouge (92)
il y a 5 jours
Sr. Manager, Statistical Programming
Ipsen Innovation (SAS) —Paris (75)
- Temps plein
- Anglais
- Niveau Licence
Clinical Data Manager Intern/apprentice F/M
Median Technologies —Valbonne (06)
- Télétravail partiel
- Pas d'expérience requise
- Anglais
- Master
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Associate Product Specialist, Monolix
Simulations Plus —Antony (92)
- De 50 000 € à 65 000 € par an
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- Niveau Doctorat
- Anglais
- Microsoft Office
Postuler rapidement
Sr. CMC, Global Project Manager
Ipsen Pharma (SAS) —Paris (75)
- Temps plein
- Niveau Doctorat
- Anglais
- Microsoft Office
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Manager, Asset Operations- Sub team Planner
Ipsen Innovation (SAS) —Paris (75)
- Temps plein
- Niveau Doctorat
- Anglais
- Niveau Licence
Clinical Data Management Lead
IQVIA —Paris (75)
- Temps plein
- Télétravail
- Oracle
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- Leadership
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Associate Product Specialist, Monolix
Immunetrics —Antony (92)
- Temps plein
- Niveau Doctorat
- Anglais
- Microsoft Office

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : clinical data manager (france)

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Experienced Clinical Research Associate, Sponsor-dedicated

IQVIA -
Paris (75)

Soumettre votre candidature

Détails de l'emploi

Temps plein

Qualifications

Français
Anglais
Leadership
Soins infirmiers

Description complète du poste

Paris, France | Full time | Hybrid | R1482470

IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.

Leadership recognizes the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.

Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties.

Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.

What we Offer:

Excellent salary and benefits package
Flexible working hours in an office-based or a home-based role in Bordeaux, Lille, Lyon, Nantes, Marseille,
We invest in keeping our teams stable, so workload is consistent
We offer genuine career development opportunities for those who want to grow as part of the organisation
We give the chance to work on cutting edge medicines, right at the forefront of new medicine development

Role Details:

Working in partnership with a single-sponsor
Usually allocated to 2-3 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
Responsible for approximately 15 sites
On site between 6 and 9 days per month, dependent on the sponsor
All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
Permanent employment contract

Responsibilities:

Site management and monitoring activities across France
Work with sites to adapt, drive and track subject recruitment plan
Provide protocol and study training to the assigned sites
Create and maintain monitoring visit reports and action plans
If appropriate, co-monitor, train and mentor junior members of the team

Become part of our team.

We believe in hiring the best talent in the industry.

To become part of our team, you should:

Have a degree in Life Sciences or have equivalent experience within a nursing background.
Have at least 2 years of independent on-site monitoring experience
Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
Have in depth GCP knowledge
Be flexible with the ability to travel nationwide
Hold a full French and clean driving license
Possess strong communication, written and presentation skills are a must (must have fluency in English and French language)
With the merger between Quintiles and IMS Health, we now have access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. It’s the next generation of clinical development

We invite you to join IQVIA™.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

#LI-LVDW1

#CRASDAJD

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

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

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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Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : clinical data manager (france)

Where you'll work

Hybrid

Culture

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