11 meilleures offres (clinical research associate, île de france) (à pourvoir)

Clinical Trial Associate
Excelya —Paris (75)
- Temps plein
- Télétravail
- Microsoft Excel
- Anglais
- Master
Postuler rapidement
Clinical Research Associate II
PSI CRO —Saint-Maur-des-Fossés (94)
- Temps plein
- Télétravail
- Anglais
- Microsoft Office
Postuler rapidement
Clinical Research Associate
Excelya —Paris (75)
- Temps plein
- Télétravail partiel
- Niveau Licence
Postuler rapidement
il y a 11 jours
Experienced Clinical Research Associate, Sponsor-dedicated
IQVIA —Paris (75)
- Temps plein
- Anglais
- Leadership
- Soins infirmiers
Freelance Senior Clinical Research Associate
TFS HealthScience —Paris (75)
- Télétravail
- Anglais
- Niveau Licence
- Soins infirmiers
Postuler rapidement
il y a 12 jours
Clinical Research Associate – Freelance | France, Spain & Italy | Oncology
TempoPHARMA —Vélizy-Villacoublay (78)
- Temps plein
- Télétravail
- Espagnol
- Anglais
Postuler rapidement
Assistant CRA - FSP - Paris region
Thermo Fisher Scientific —Saint-Aubin (91)
- Temps plein
- Service client
- Anglais
- Microsoft Office
Intern CRA - FSO
Fortrea —Paris (75)
- Temps plein
- Niveau Licence
CRA II in MultiSponsor - Based in Paris Office
サイネオス・ヘルス —Paris (75)
- Master
- Niveau Licence
CRA I - FSP - Paris region
Thermo Fisher Scientific —Saint-Aubin (91)
- Temps plein
- Anglais
- Microsoft Office
- Niveau Licence
Cracking the code of GTPBP3/MTO1: Structural and Functional characterization and links to rare human diseases
Sorbonne Université —Paris (75)
- Niveau Doctorat
- Anglais
- Master

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Clinical Trial Associate

Excelya -
Paris (75)

Postuler rapidement

Détails de l'emploi

Temps plein

Qualifications

Microsoft Excel
Anglais
Master
Expérience administrative
Niveau Licence
SharePoint
Compétences en communication

Description complète du poste

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Key responsibilities :

Manage and maintain the Trial Master File (TMF/eTMF), ensuring completeness, accuracy, compliance, and inspection readiness throughout the study lifecycle.
Coordinate TMF documentation activities, including collection, filing, tracking, and reconciliation of study documents from internal teams and CROs.
Conduct TMF quality reviews and QC checks to ensure compliance with ICH-GCP requirements and company procedures.
Ensure timely identification and resolution of missing, outdated, or incomplete study documentation.
Oversee study document archiving activities in accordance with regulatory and company requirements.
Support financial management of clinical studies, including purchase orders, invoices, budget tracking, commitments, and payment follow-up.
Coordinate transparency reporting activities and maintain documentation required for compliance with local and international disclosure regulations.
Provide operational support for clinical studies, including contract management, insurance renewals, clinical supply coordination, and maintenance of essential legal documents.
Maintain and update clinical systems and tracking tools (CTMS, SAP, SharePoint, iCap, and related platforms) to ensure accurate study status reporting.
Act as a key operational liaison between Clinical Research Managers, CROs, vendors, and internal stakeholders, supporting the successful delivery of clinical trials within quality, timeline, and regulatory requirements.

Requirements

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biology, Health Sciences, or a related field.
Experience in Clinical Operations, Clinical Trial Management support, Trial Master File (TMF/eTMF) management, or Clinical Research Administration within the pharmaceutical, biotechnology, or CRO environment. Strong knowledge of ICH-GCP guidelines, clinical trial processes, and applicable regulatory requirements. Managing and maintaining TMF/eTMF systems, ensuring inspection readiness and document quality compliance.
Proven ability to coordinate multiple stakeholders, including CRMs, CROs, vendors, investigators, and internal departments.
Experience with financial and administrative aspects of clinical studies, including budget tracking, purchase orders, invoices, and financial systems.
Familiarity with clinical systems and tools such as CTMS, eTMF platforms, SAP, SharePoint, and document management systems.
Strong organizational skills with the ability to manage multiple priorities and meet deadlines in a fast-paced environment.
Excellent command of Microsoft Excel with advanced data analysis and reporting skills.
Effective written and verbal communication skills, with the ability to work collaboratively in an international and cross-functional environment.
Fluent in English

Benefits

Why join us?

At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.

Here's what makes us unique:

We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.

Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.

Excelling with kindness means evolving in an environment that values your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.

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clinical research associate emplois - île de france

Clinical Trial Associate

Clinical Research Associate II

Clinical Research Associate

Experienced Clinical Research Associate, Sponsor-dedicated

Freelance Senior Clinical Research Associate

Clinical Research Associate – Freelance | France, Spain & Italy | Oncology

Assistant CRA - FSP - Paris region

Intern CRA - FSO

CRA II in MultiSponsor - Based in Paris Office

CRA I - FSP - Paris region

Cracking the code of GTPBP3/MTO1: Structural and Functional characterization and links to rare human diseases

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : clinical research associate (île de france)

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