Flychem is looking for an experienced qualified 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.

📌 Scientific Studies (Hyderabad)
🏢 FlyChem
📍 Hyderabad