# Medical Affairs Consultant

> Digital · India (Remote) · Temporary · Posted 2026-07-03

**Workplace:** remote

**Department:** Hire Digital

## Description

Hire Digital is seeking a **Medical Affairs Consultant – Claims Substantiation** with an APAC market focus to update and strengthen the internal claims matrix that underpins two of its flagship products, RADIESSE® and ULTHERAPY®. This role will focus on reviewing and appraising clinical evidence, determining which product claims can be safely substantiated, and refining claim language for both healthcare professional (HCP) and consumer-facing use with particular attention to APAC-specific publications and the broader regional evidence base.

This is an ideal opportunity for professionals with experience in medical affairs, medico-legal review (MLR), regulatory affairs, or scientific and medical communications who understand how clinical evidence supports promotional claims and can translate complex data into clear, compliant, and commercially useful recommendations.

### Responsibilities

-   Lead the end-to-end review, update, and expansion of the RADIESSE® and ULTHERAPY® claims matrix, which serves as the internal source of truth for substantiating product claims across marketing, medical education, and HCP engagement.
-   Conduct structured literature reviews to identify relevant new publications not yet captured in the matrix, including APAC-specific clinical studies, real-world evidence, and consensus papers.
-   Critically appraise the quality, strength, and relevance of the clinical evidence behind each claim, applying recognised levels-of-evidence and evidence-grading principles.
-   Determine which claims can be made safely and which require stronger support, clearly distinguishing what is defensible for HCP-facing versus consumer-facing use.
-   Refine claim wording so it is scientifically accurate, clear, and appropriately caveated, including careful handling of superiority and "first/only" style claims.
-   Establish a clear claim hierarchy and identify differentiating or competitive claims that are genuinely supported by the evidence.
-   Validate all references and build a complete, well-organised reference library and source-documentation trail.
-   Identify evidence gaps and recommend priority claims and future evidence-generation opportunities.
-   Ensure the matrix and its recommendations align with medico-legal / regulatory review standards and the client's internal review and approval processes.
-   Present findings and recommendations clearly to medical, marketing, and regulatory stakeholders.

## Requirements

_Essential_

-   Hands-on experience in medical or scientific claims review, medico-legal review (MLR), regulatory affairs, or medical affairs within pharmaceuticals, medical devices, or aesthetics.
-   Strong critical-appraisal skills and confidence working with clinical literature (study design, endpoints, statistics, and evidence grading).
-   Experience conducting literature reviews and validating references.
-   A solid grasp of the principles governing promotional claims, and how substantiation standards differ for HCP versus consumer communications.
-   Excellent scientific writing, with a sharp eye for accuracy and detail.

_Desirable_

-   Familiarity with aesthetics, dermatology, injectables, or energy-based devices.
-   Awareness of APAC regulatory nuances, local codes of practice, and regional evidence.

## Apply

[Apply at Digital](https://apply.workable.com/digital-368/j/3AE56D39C8/apply)

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