Кирилл Х.

Key Skills

Software

Other

Top Subject Matter

Medical/Pharmaceutical clinical research documentation and regulatory writing

Medical/Pharmaceutical clinical research documentation

Medical Writer & Clinical Data Evaluation Specialist

Top Data Types

Document

Text

Top Task Types

Text Generation

Evaluation/Rating

Classification

Text Summarization

Data Collection

Freelancer Overview

Medical Doctor and Medical Writer with 10+ years of experience in clinical research documentation, regulatory writing, and critical evaluation of scientific data. Specialized in synthesizing complex medical and pharmacological information from global literature into structured outputs (CTD modules, clinical overviews, benefit-risk assessments). Strong expertise in evidence-based medicine, pharmacokinetics, safety evaluation, and multilingual literature review. Open to contributing medical domain knowledge to AI training, evaluation, summarization, and medical content generation projects.

Labeling Experience

Assistant Clinical Investigator / Junior Medical Writer (Innopharmatech CRO) — foundational clinical trial documentation support

OtherDocumentText Generation

Assisted clinical trial documentation development by supporting structured scientific writing and critical evaluation of clinical trial materials. Contributed to preparation of regulatory-related trial documents while learning core methods for evidence-based documentation. Applied medical domain understanding to help convert trial information into readable, organized outputs suitable for downstream regulatory and research workflows. • Support clinical trial execution documentation • Junior medical writing and structured scientific summaries • Foundational critical evaluation of trial materials • Preparation support for regulatory documents

2016 - Present

Medical Writer (Chemical Diversity Research Institute, CDRI) — clinical/regulatory evidence synthesis and documentation authoring

OtherDocumentText Generation

Produced structured medical and regulatory documentation by synthesizing clinical, pharmacological, and safety evidence into CTD Module sections and benefit-risk assessments. Performed critical appraisal of study findings (efficacy, safety, pharmacokinetics/pharmacodynamics, toxicology) and converted sources into evidence-based narrative outputs. Adapted and translated multilingual scientific literature to support compliant medical/regulatory writing and research use cases. • CTD Module 2.4–2.7 regulatory document preparation • Benefit-risk assessment writing and evidence synthesis • Multilingual literature search, translation, and adaptation • Protocols, Investigator Brochures, and Informed Consent Form authoring

2016 - Present

Education

Work History