Cdi - Clinical Trial Administration Specialist F/m

Il y a 6 mois


Lyon, France bioMérieux sa Temps plein

A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to **improve public health**. Today, our teams are spread across 45 countries and serve 160 countries with the support of a large distribution network.
Come and join a family-owned global company with a long-term vision, and a human-centered culture.

**What are your main accountabilities ?**

We are seeking a Clinical Trial Administration Specialist to join our bioMérieux Clinical Affairs team. In a corporate department, you will work with a global team of about 30 Clinical Scientists located in France and in the USA.

This position is necessarily based in Marcy l’Etoile site.

As Clinical Trial Administration Specialist, you will assist and support the conduct of clinical trials related administrative activities as per clinical project timelines. You will act as a liaison person between external Clinical Trial sites, Clinical Scientists and other internal departments.
- Assist in trial Confidential Disclosure Agreements and Agreements preparation with bioMérieux Legal department and the external clinical trial sites,
- Prepare templates for budget estimates and facilitates communication between internal and external partners during contract and budget phases of the Clinical Trial project,
- Manage the clinical sites/external providers referencing, purchase orders, invoicing processes, regular accruals,
- Prepare the documentation package for the purpose of the submission to Independent Ethic Committee or Independent Review Board, as per respective expectations,
- Report any clinical trial related relevant information to competent authorities (e.g. Sunshine act...),
- Maintain the clinical trial related documentation ahead, during and after the completion of the clinical trial, collaboratively with the Clinical Scientist, along with the clinical sites,
- Prepare the on-site documentation as per Good Clinical Practices (Investigator Study File - ISF),
- Structure, prepare and regularly feed the electronic clinical trial master file, including all the trial documentation and main project deliverables.

**What is your profile?**
- BAC+2 level or equivalent required, plus 3-5 years in the industry, ideally with a clinical research background
- Excellent oral and written communication in English
- Skills in administrative tools (Office 365, Teams, Outlook,), WebApp. SAP knowledge is a plus.
- Basic knowledge in biology or Medical devices would be a nice to have
- Pro-active attitude and able to take initiatives
- Team spirit and collaborative work among peers and with department members
- Excellent sense of service, good sense of adaptation, great organizational, ability to prioritize, rigor, methodical approach


  • Clinical Trial Assistant

    Il y a 6 mois


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management team in Lyon. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...

  • Clinical Trial Manager

    Il y a 3 mois


    Lyon, France ADOCIA Temps plein

    Adocia is a French clinical-stage biotech company. The core activities of the company are to innovate, to discover and to develop new therapeutic solutions to improve the lives of people suffering from chronic metabolic diseases, such as diabetes and obesity. Adocia innovative products share a common goal: to improve treatments, bringing new medical benefits...

  • Clinical Trial Manager

    il y a 2 semaines


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Lyon. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to expand to a...


  • Lyon, France Medpace, Inc. Temps plein

    Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management team in Lyon. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success and is suited for an Entry-level or recent graduate...


  • Lyon, France Medpace Temps plein

    **Responsibilities **- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact with the...


  • Lyon, France Medpace, Inc. Temps plein

    Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

  • Clinical Trial Assistant

    Il y a 6 mois


    Lyon, France Aixial Temps plein

    Vous êtes passionné(e)s par le monde des sciences de la vie et de la recherche clinique ? Vous souhaitez évoluer dans un environnement international dynamique et collaboratif où votre expertise a un impact direct sur la vie des millions de personnes ? Rejoignez Aixial Group et contribuez à façonner l’avenir de la recherche clinique ! **Qui...


  • Lyon, France Medpace, Inc. Temps plein

    Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...


  • Lyon, France EastHORN Clinical Services Temps plein

    **Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....


  • Lyon 7e, France AUROBAC THERAPEUTICS Temps plein

    **Presentation of the company**: AUROBAC THERAPEUTICS is a biopharmaceutical company created in 2022 by 3 renowned life sciences innovation companies, Boehringer Ingelheim, Evotec and bioMérieux, to become a global leader in the fight against bacterial infections, Antimicrobial Resistance (AMR) and their consequences in acute hospital settings such as...


  • Lyon, France Excelya Temps plein

    I. Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging...


  • Lyon, Rhône, France Excelya Temps plein

    I. Excelya Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging...

  • Clinical Data Manager

    Il y a 3 mois


    Lyon, France Amaris Consulting Temps plein

    Job description We are seeking a skilled and dedicated Clinical Data Manager to join our team at Amaris Consulting - CRO. As a Clinical Data Manager, you will be responsible for overseeing the data management activities for clinical trials and research projects. You will work closely with cross-functional teams to ensure...


  • Lyon, France Medpace Temps plein

    Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing France team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success....


  • Lyon, Auvergne-Rhône-Alpes, France Excelya Temps plein

    Our MissionWe are looking for a highly organized and detail-oriented individual to join our team as a Clinical Trial Assistant. In this role, you will provide administrative and regulatory support for clinical trials, ensuring seamless execution and compliance with regulations.Key Responsibilities:Provide administrative support for clinical trials, including...

  • Regulatory Specialist

    Il y a 6 mois


    Lyon, France EastHORN Clinical Services Temps plein

    **Job summary**: As a **Regulatory Specialist **you will be expected to actively participate in all start up activities and perform CA and EC submissions. You will be responsible for communication with Regulatory Authorities and Ethics Committees and function as an expert for Regulatory issues in France. Reporting to **Clinical Operations Manager**, you will...

  • Clinical Research Associate

    il y a 4 semaines


    Lyon, Auvergne-Rhône-Alpes, France Pharmiweb Temps plein

    InHouse Clinical Research Associate - An opportunity to shape the future of clinical development with ICON plc, a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence. Key Responsibilities: Support the execution and management of clinical trialsConduct site feasibility...


  • Lyon, Auvergne-Rhône-Alpes, France M2TALENTS Temps plein

    Unlock Your Potential in Medical ResearchM2TALENTS is a leading partner for innovative career opportunities, and we're excited to offer a unique chance to advance your career as a Senior Clinical Research Specialist.About the Role:As a Senior Clinical Research Specialist, you'll play a vital role in supporting medical projects, including experimental and...


  • Lyon, France Amolyt Pharma Temps plein

    Nous poursuivons aujourd’hui notre développement et la structuration de nos équipes en France et aux USA afin d’avancer le développement de nos programmes et renforcer notre portefeuille de produits. Pour soutenir l’ensemble de notre équipe clinique et rattachée à notre Directrice des opérations cliniques, nous ouvrons donc un poste...


  • Lyon, France Proclinical Temps plein

    Proclinical are recruiting for a Senior Clinical Research Associate for a CRO. This role is on a permanent basis and is located in France. *** **Responsibilities**: - Perform qualification, initiation, supervision and close-out visits for research sites in compliance with the approved protocol. - Guarantee GDP are being adhered to and discussing protocol...