Open to opportunities

Abdul Rahman Ashik

@abdulrahmanashik

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Medical writer specializing in regulatory and scholarly writing with evidence synthesis expertise.

India

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What I'm looking for

I seek a role leveraging regulatory and scholarly medical writing skills, with collaborative, GxP-compliant teams, opportunities for evidence synthesis and publication work.

I am a medical writer with ~2 years of hands-on experience in regulatory and scientific writing, focused on clinical evaluation, literature synthesis, and quality documentation.

I transform complex clinical and safety data into clear, publication-ready and regulatory-ready narratives, working within regulated environments (GxP, ISO, ICH) and collaborating with multidisciplinary teams.

My core achievements include authoring and reviewing Clinical Evaluation Reports (CER) compliant with EU MDR 2017/745, conducting systematic literature searches and evidence synthesis using PubMed, Embase and OVID, and preparing conference-ready scientific materials.

I bring strong experience in quality and compliance (EU MDR, ICH guidelines, ISO 14971), reference management (EndNote, Zotero, Mendeley), and systematic review tools (DistillerSR), aiming to produce audit-ready documentation and rigorous, transparent scientific outputs.

Experience

Work history, roles, and key accomplishments

Current

Medical Writer

Current

HCLTech Limited

Sep 2024 - Present (1 year 5 months)

Author and review Clinical Evaluation Reports (CER) and related clinical documentation compliant with EU MDR 2017/745; conducted systematic literature searches and evidence synthesis to produce publication- and regulatory-ready narratives.

Regulatory Writing Clinical Evaluation PubMed Prisma CONSORT Medical Editing

Documentation Analyst

Archimedis Digital

May 2024 - Sep 2024 (4 months)

Prepared and reviewed SOPs, APQRs, and controlled documents supporting GxP-compliant documentation and document lifecycle management for inspection-ready readiness.

Change Control Document Management

Quality Assurance Trainee

Apotex Research Private Limited

Sep 2023 - Feb 2024 (5 months)

Supported GMP documentation including SOPs, BMRs, and MFRs and assisted in audit documentation for FDA and MHRA internal inspections, building foundational regulated documentation skills.

GMP Documentation SOPs Audit Support Regulatory Compliance