Regulatory Medical Claims Consultant (Aesthetics)

Hire Digital is looking for a consultant to support the development of a structured medical claims governance and evidence substantiation framework across its product portfolio. The Regulatory Medical Claims Consultant will be responsible for reviewing, validating, and governing scientific claims used across key aesthetic products. The role will define the framework for how claims are assessed, structured, and approved based on clinical evidence and regulatory requirements. This role sits within the intersection of Regulatory Affairs, Medical Affairs, and Clinical Evidence Review, ensuring all scientific claims used across medical, marketing, and HCP communications are fully substantiated, compliant, and aligned with internal MLR standards. This is a scientific and regulatory decision-making role, not a content writing position. RESPONSIBILITIES Lead the review and validation of scientific and clinical claims across medical aesthetics products. Conduct structured assessment of clinical literature, real-world evidence, and consensus publications. Identify and evaluate relevant global and APAC-specific evidence supporting product claims. Ensure all claims are scientifically accurate, appropriately substantiated, and regulatorily compliant. Define and implement a claims governance framework and evidence grading system. Categorise claims based on strength of evidence (high / moderate / exploratory). Determine appropriate claim usage across HCP and consumer-facing materials. Ensure alignment of all claims with internal Medical-Legal-Regulatory (MLR) processes. Identify gaps in clinical evidence and recommend future substantiation strategies. Develop and maintain a structured claims matrix and supporting reference library . REQUIREMENTS Experience in Regulatory Affairs, Medical Affairs, Medical Information, or MLR (Medical-Legal Review). Proven experience reviewing or approving promotional or scientific claims in a regulated environment. Strong understanding of clinical literature, evidence evaluation, and scientific interpretation. Experience in pharma, medical devices, dermatology, or medical aesthetics preferred. Familiarity with regulatory frameworks and evidence grading methodologies. Ability to operate across cross-functional teams (Medical, Regulatory, Marketing). Strong analytical thinking and structured decision-making capability.