
Medical Affairs Consultant
Posted Jul 18

Posted Jul 18
This is a fully remote position, open to applicants in India.
⢠Oversee the comprehensive review, updating, and enhancement of the RADIESSE® and ULTHERAPY® claims matrix, which acts as the definitive internal resource for substantiating product claims across marketing, medical education, and healthcare professional (HCP) engagement.
⢠Perform structured literature reviews to discover pertinent new publications that have not yet been included in the matrix, encompassing APAC-specific clinical studies, real-world evidence, and consensus papers.
⢠Evaluate the quality, strength, and relevance of the clinical evidence supporting each claim, utilizing recognized levels-of-evidence and evidence-grading principles.
⢠Assess which claims can be confidently made and which necessitate stronger backing, clearly differentiating between what is defensible for HCP-facing and consumer-facing applications.
⢠Fine-tune claim language to ensure it is scientifically precise, clear, and suitably caveated, including careful management of superiority and "first/only" type claims.
⢠Create a definitive claim hierarchy and pinpoint differentiating or competitive claims that are genuinely substantiated by the evidence.
⢠Authenticate all references and develop a comprehensive, well-structured reference library along with a source-documentation trail.
⢠Identify gaps in evidence and provide recommendations for priority claims and future evidence-generation opportunities.
⢠Ensure that the matrix and its recommendations comply with medico-legal and regulatory review standards as well as the client's internal review and approval processes.
⢠Clearly present findings and recommendations to medical, marketing, and regulatory stakeholders.
⢠Practical experience in medical or scientific claims review, medico-legal review (MLR), regulatory affairs, or medical affairs in the pharmaceutical, medical device, or aesthetics sectors.
⢠Strong critical appraisal abilities and confidence in working with clinical literature (study design, endpoints, statistics, and evidence grading).
⢠Experience in conducting literature reviews and validating references.
⢠A solid understanding of the principles that govern promotional claims and the differences in substantiation standards for HCP versus consumer communications.
⢠Exceptional scientific writing skills, with a keen eye for accuracy and detail.
⢠Familiarity with aesthetics, dermatology, injectables, or energy-based devices.
⢠Knowledge of APAC regulatory nuances, local codes of practice, and regional evidence.
⢠Competitive salary and performance-based bonuses.
⢠Comprehensive health benefits package.
⢠Opportunities for professional development and continuous learning.
⢠Collaborative and innovative work environment.
ToxStrategies, a BlueRidge Life Sciences Company
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