- Medical/Science Communication: content development, review, editing and proof-reading of medical/scientific and marketing material.- Clinical Trials: study proposal, trial management, clinical operations.- Regulatory & Medical Affairs.- New Product Development: formulation proposal and development, from idea generation to product launch.- Training and Education: content development, review and proof-reading of educational presentations for various audiences (professionals, lay public, sales force)

- R&D team management.- R&D budget management.- Preparation and drafting of research proposals and grants.- Design, supervision, invigilation, analysis and reporting of scientific studies and clinical trials to be carried out with research institutes, aesthetic medicine specialists or cosmetic dermatologists.- Preparation of technical documentation for ethical committee approval and submission to the specific bodies (for example, HRA approval for clinical trials based in UK).- Scientific literature research and review followed by the preparation of manuscripts, reports and scientific dossiers to submit to appropriate peer-reviewed high IF journals.- Research and review of relevant literature defining EU and National regulations supporting the release of nutraceutical product and health claims. - Preparation of technical and regulatory documents to support registration of products with different authorities including EFSA, MHRA, FDA.- New product development and existing product evolution: formulation proposal, development, validation and testing. - Liaison with external stakeholders, partners and suppliers including: Universities; Research Institutes; Clinical Trial Specialists and Investigators; Doctors/Aesthetic Medicine Specialist/Cosmetic Surgeons; Ingredient Manufactures; Pharmaceutical Contract Manufacturers; Pharmaceutical Bodies/Agencies/Specialists; European/National Regulatory Bodies and Regulatory Specialists/Consultants.

• Design, supervision, invigilation, analysis and reporting of scientific studies and clinical trials to be carried out with research institutes, aesthetic medicine specialists or cosmetic dermatologists.• Collaboration with external stakeholders to perform clinical trials.• Collaboration with ingredient manufacturers, research labs, aesthetic medicine specialists and doctors.• Scientific Literature research and review followed by the preparation of manuscripts, reports and scientific dossiers to submit to appropriate peer-reviewed high IF journals.• Research and review of relevant literature defining EU and National regulations supporting the release of nutraceutical product and health claims. • Preparation of technical and regulatory documents to support registration of products with different authorities including EFSA, MHRA, FDA.• New product development and existing product evolution: formulation proposal, development, validation and testing. • Liaison with MINERVA’s partners and suppliers including: Universities; Research Institutes; Clinical Trial Specialists and Investigators; Doctors/Aesthetic Medicine Specialist/Cosmetic Surgeons; Ingredient Manufactures; Pharmaceutical Contract Manufacturers; Pharmaceutical Bodies/Agencies/Specialists; European/National Regulatory Bodies and Regulatory Specialists/Consultants.• Analysis of competitor products.• Team management.

- Invigilation, analysis and reporting of scientific studies to be carried out with aesthetic medicine specialists or cosmetic dermatologists.- Collaboration with external stakeholders to perform clinical trials along with in-vivo and in-vitro experiments.- Collaboration with ingredient manufacturers, research labs and aesthetic medicine technology (laser and RF).- Scientific Literature research and review followed by the preparation of papers, reports and scientific dossiers in the space of anti-ageing nutrition, cosmetic dermatology and aesthetic medicine.- New product development: formulation proposal, development, validation and testing.- Existing product evolution: formulation proposal, development, validation and testing.- Liaison with MINERVA’s partners and suppliers including: Universities; Research Institutes; Clinical Trial Specialists and investigators; Doctors/Aesthetic Medicine Specialist/Cosmetic Surgeons; Ingredient Manufactures; Pharmaceutical Contract Manufacturers.- Analysis of competitor products.