Hire Digital is looking for a consultant to support a strategic initiative focused on strengthening its internal claims matrix and evidence substantiation framework across key product portfolios.

The Medical Claims & Evidence Substantiation Consultant will be responsible for reviewing, validating, and structuring scientific claims used across medical aesthetics products. The role ensures that all claims are scientifically accurate, appropriately supported by clinical evidence, and aligned with internal MLR (Medical-Legal-Regulatory) standards. This role sits at the intersection of Medical Affairs, Regulatory Affairs, and Clinical Evidence Review, ensuring all scientific claims used across marketing, HCP communications, and internal materials are fully substantiated, compliant, and evidence-backed.

This is not a content writing role. It requires strong expertise in medical affairs, regulatory review, and clinical evidence interpretation.

Requirements

RESPONSIBILITIES

• Conduct structured literature reviews across clinical trials, real-world evidence, and consensus publications.
• Identify and evaluate new global and APAC-specific scientific publications relevant to product claims.
• Review and validate existing claims for scientific accuracy and robustness.
• Assess strength and quality of supporting clinical evidence for each claim.
• Categorise claims by level of evidence (high / moderate / exploratory).
• Define appropriate usage of claims across HCP and consumer-facing communications.
• Ensure all claims align with internal MLR and regulatory compliance requirements.
• Refine claim language for clarity, consistency, and scientific accuracy.
• Develop and maintain a structured claims matrix and supporting reference library.
• Identify gaps in evidence and recommend areas for future substantiation.

REQUIREMENTS

• Experience in Medical Affairs, Medical Information, Regulatory Affairs, or MLR (Medical-Legal Review).
• Proven exposure to promotional material review or scientific claims evaluation.
• Strong ability to interpret and assess clinical literature and evidence quality.
• Experience working in pharma, medtech, dermatology, or medical aesthetics preferred.
• Familiarity with evidence grading frameworks and regulatory requirements.
• Ability to operate in a cross-functional environment (medical, regulatory, marketing).
• Strong attention to detail and structured, analytical thinking.