Responsible for designing, planning and monitoring FILORGA Cosmetics' global cosmetic clinical studies and ensuring that investigators conduct studies in accordance with clinical protocol requirements ensuring:
- The research is conducted in accordance with applicable regulations / European regulations and its guidelines.
- IRB parameters / journal publications requirements for EU are met.
- Protocol meets the needs of the R&D & Marketing Departments and supports claims made on the product.
- The rights and safety of human subjects involved in a clinical study are protected through a Consent Form in local language (where study will be conducted) and in English.
Additional details:
-Responsible for independently managing relationships and liaising with CROs/testing labs and the team; expanding network of sites to fulfill new claims requirements.
-Ensures GCP and regulations are followed as well as management of undesirable events, serious or not, concerning Filorga's cosmetic projects.
-Trains and informs investigators and participants in studies for Filorga's cosmetic projects.
-Manages data collected by CROs/testing labs, contributes to interpretation of data/conclusions and reviews final report.
-Ensures administrative and logistical follow-up of study documents and shares clinical study results with all concerned.
-Leads portfolio analysis of product clinical studies and scientific evidence to benchmark / understand efficacy strengths and gaps.
-Contributes to content information for Sales force training, media presentations and supports scientific communications to retailers, congresses, etc.
-Participates in writing & submitting peer review publications to journals, delivering posters & presentations to conferences/congresses.
-Organizes & leads Filorga Cosmetics scientific committees/Advisory Board meetings (agenda, invitation, follow-ups, etc.).
-Participates in the organization of press conferences & presents scientific/clinical studies.
-Ph.D. (Science, Clinical/Medical field) or pharmacist level with relevant experience
-At least 5 years functional experience required.
Moderate/Strong experience in clinical research preferred (preferably in Personal Care products)
-Experience in submissions to peer reviewed publications, international congresses and liaising with skin health professionals.
-Fluent in French and English (verbal and written).
-Dynamic, proactive person who wants to invest in a fast growing company & is a team player.
Location: Paris, France