What are your responsibilities?

To participate to Phase I-IV Clinical Development activities within a program or group of related programs within the context of the internal process in order to ensure the high quality and on-time delivery of all clinical data that will allow world-wide registration in compliance with the clinical development plan, good clinical practices (GCP), and internal standard operating procedures (SOP).
Key Responsibilities:

1. Participate in Clinical Development activities for a study or a number of studies within a specific program or group of related programs.
2. Serves as a scientific and management reference for the project (internally/externally)
3. As a member of the Clinical Project Team, always actively participate and engage within the project matrix.

4. Actively participate in preparing the clinical portion of the regulatory files and the registration process

5. Provides support to Marketing/Business Development throughout product life cycle

6. Show active follow-up the product-related Environment

What skills do you bring to the table?

• Master degree or PhD
• Ability to independently research questions; sound scientific background required to critically evaluate all scientific aspects of vaccinology / immunology.
• Previous experience in the field of pediatrics, obstetrics and gynecology, infectious diseases, clinical epidemiology, pharmacoepidemiology, and/or clinical vaccinology is an asset.
• Min years’ experience required: 2-5 years
• Fluent in English

What’s the offer you can’t refuse?

As an Akkodis Team Member, you will be:

• Onboarded in your position via a buddy process
• Supported in your career by your Business Manager
• Actor of your training plan and your personal and professional development
• Benefiting from a permanent contract
• Benefiting from a competitive salary package including several extra-legal benefits

Do you any questions? You can contact me at marie.defruit@akkodis.com