Scientific Studies & Clinical Validation Consultant

Flychem is looking for an experienced professional to independently plan, coordinate and review scientific efficacy and safety studies for cosmetic and personal-care ingredients and formulations. The consultant will work remotely and support multiple studies on a flexible, part-time basis.

Key Responsibilities
• Plan in-vitro, ex-vivo and human clinical studies based on product claims and mechanisms of action.
• Identify, evaluate and coordinate with suitable CROs, laboratories, dermatologists and research institutes.
• Develop and review study protocols, endpoints, testing methodologies and sample-size requirements.
• Coordinate efficacy, safety, dermatological and instrumental testing.
• Monitor study timelines, budgets, documentation and CRO deliverables.
• Review raw data, statistical analysis and final study reports.
• Translate study outcomes into scientifically substantiated product claims.
• Prepare technical study summaries, claim-support documents and scientific presentations.
• Guide R&D;, Regulatory and Marketing teams on suitable studies for new ingredients and finished formulations.
• Track relevant study standards, testing methodologies and global claim-substantiation requirements.

Preferred Profile
• M.Pharm / Pharm.D / MSc / PhD in Pharmacology, Biotechnology, Life Sciences, Pharmacy or a related discipline.
• 5+ years of relevant experience in clinical research, CRO management, cosmetic efficacy testing, dermatological studies or claim substantiation.
• Strong understanding of in-vitro, ex-vivo and human clinical study design.
• Ability to independently review protocols, statistical outputs and technical reports.
• Prior experience with cosmetics, dermatology, pharmaceuticals or personal-care products is preferred.

Role Objective

Take ownership of the complete study cycle: study concept -> protocol -> CRO selection -> execution -> data review -> final report -> claim substantiation.