Radhika M.

Key Skills

Software

Other

Don't disclose

Top Subject Matter

Clinical validation of device studies and AI-assisted medical content for regulatory evaluation (EU MDR/ISO

. Domain Expertise

Evidence-based medical/clinical content review and regulatory dossier accuracy validation (MLR, FDA, ABPI).

Top Data Types

Text

Document

Image

Top Task Types

Diagnosis

Freelancer Overview

Clinical Evidence Evaluation Specialist | LivaNova PLC. Brings 10+ years of professional experience across legal operations, contract review, compliance, and structured analysis. Core strengths include Internal, Proprietary Tooling, and Don't disclose. Education includes Master of Dental Surgery, Rajiv Gandhi University of Health Sciences (2017) and Bachelor of Dental Surgery, Maharashtra University of Health Sciences (2012). AI-training focus includes data types such as Medical, DICOM, and Document and labeling workflows including Evaluation, Rating, and Diagnosis.

Labeling Experience

Clinical Evidence Evaluation Specialist — LivaNova PLC (Nov 2023 - Feb 2025).

Text

Reviewed and validated clinical data outputs and AI-assisted content for scientific accuracy, relevance, and regulatory readiness, acting as a verifier of model-generated ground truth. Flagged inaccuracies and provided structured written feedback within internal validation workflows similar to correcting labels produced by AI systems. Produced evidence-backed clinical evaluation reports by cross-checking outputs against source data and published literature. • Validated device study clinical data outputs for correctness and compliance readiness. • Reviewed AI-assisted content and data outputs in structured internal workflows. • Authored and verified clinical evaluation reports, summaries, and manuscripts aligned to evidence. • Conducted literature reviews to support clinical evaluation reports under EU MDR and ISO 14155.

2023 - 2025

Senior Associate - Medical Writer & Reviewer — Indegene Pvt. Ltd. (Feb 2021 - Oct 2022).

OtherDocument

Authored and reviewed medical and scientific documents including regulatory dossiers and promotional materials, performing accuracy, consistency, and compliance checks against referenced evidence. Led end-to-end Medical-Legal-Regulatory (MLR) review workflows that validated scientific claims, data integrity, and required alignment with FDA and ABPI standards. Performed systematic literature searches and created clinical trial summaries and abstracts to support validated content generation for regulated use. • Reviewed and authored standard response documents, slide decks, Q&As, manuscripts, brochures, and regulatory dossiers across therapy areas. • Conducted MLR reviews to validate scientific accuracy and data consistency for FDA/ABPI compliance. • Performed literature searches (PubMed/EMBASE) and developed evidence summaries and abstracts. • Mentored reviewers in evidence-based validation and scientific writing standards.

2021 - 2022

Associate Dentist | Glow Dent Oral Health Clinic

Don't discloseImageDiagnosis

Conducted clinical examinations supported by dental radiograph interpretation to establish diagnostic ground truth. Developed personalized treatment plans based on interpreted imaging findings and patient history records. Maintained highly accurate clinical documentation to support follow-ups and auditability. • Interpreted dental radiographs and intraoral findings for diagnosis • Documented patient records with audit-ready accuracy • Identified oral submucous fibrosis cases for early detection workflows • Performed tobacco-cessation counseling and specialist referral coordination

2017 - 2021

Education

Work History