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Clinical Research Associate H/F bioMérieux
- Marcy-l'Étoile - 69
- CDI
- Télétravail partiel
- Bac +2
- Industrie Pharmaceutique • Biotechn. • Chimie
- Exp. 1 à 7 ans
Les missions du poste
We are looking for a Clinical Research Associate who will work and grow within the Medical Evidence Generation department and will report to Director, Clinical Research Scientists, in a team of five co-workers.
The position is offered under an open-ended contract and is based in Marcy L'Etoile - with travels across France (~5%) and international (~5%).
What will your responsibilities be?
You lead the execution of the clinical studies that make up the company's clinical evidence generation program. In this role, you will execute clinical studies and/or programs worldwide in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures.
You collaborate closely with cross-functional teams, including Medical scientists, DM/biostats, Medical Writers, marketing, to generate impactful clinical evidence that supports the company's strategy. This role is crucial in maintaining our commitment to scientific excellence and patient-centric approaches within the competitive global healthcare landscape.
Your main missions will be the following:
* Prepare and plan clinical studies
* Develop or contribute to the Clinical Monitoring Plan, monitoring tools
* Oversee and coordinate all aspects of the clinical monitoring and site management process with adequate level of autonomy in regards of the study type
* Conduct remote or on-site visits to assess protocol and regulatory compliance and manage necessary documentation.
* Ensure compliance with relevant regulations and Good Clinical Practices
* Develop collaborative relationships with investigational sites.
* Review clinical data (e.g. electronic case report forms, central laboratory data, risk-based monitoring outputs, etc...) to ensure the management of their site's data with quality and integrity
* Support the maintenance of the relevant documents that pertain to contracts, invoices, and budgets.
* Resolve data discrepancies
* Contribute to develop and update best practices and processes
Le profil recherché
Who are you?
* You hold a Bachelor's Degree in Biology, Microbiology, or healthcare related field.
* You bring 2 years of experience in medical or clinical research, life sciences or a related function.
* You demonstrate strong capabilities in clinical study monitoring.
* You are fluent in English.
* You are willing to travel approximately 10% of the time.
Les avantages
- Matériel de qualité
- Aménagement des locaux
- Parking gratuit à proximité
- Proche transport en commun
- Locaux modernes
- Restaurant d'entreprise
- 13ème mois
- Bonne mutuelle
- Intéressement ou participation
- Prime sur objectifs
- indemnité transports
- Plan d'Epargne
- Compte Epargne Temps
- Plan d'actionnariat
- Flexibilité des horaires
- RTT
- Télétravail
- Activités sportives
- Accord Qualité de Vie au Travail
- Conciergerie
- Conciergerie médicale
- Programme d'assistance aux collaborateurs
- Programme d'échanges (maison et séjours linguistiques pour enfants)
Les étapes de recrutement
Les étapes de recrutement peuvent varier selon l'offre à laquelle vous postulez.
-
Entretien téléphonique ou vidéo avec le recruteur
-
Entretien physique avec le recruteur et le manager
-
Questionnaire de personnalité et/ou un test d'anglais (selon le poste)
-
bioMérieux en images
Publiée le 06/02/2026 - Réf : 56118 43955163
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Clinical Research Associate H/F
- Marcy-l'Étoile - 69
- CDI
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