Scientific Consultant & Medical Writing

• Scientific & Strategic Advisory

  • Target identification and preclinical strategy

  • Literature reviews and competitive landscape analysis

  • Scientific platform positioning and narrative development

• Translational & Clinical Support

  • Clinical development insights for early-phase programs

  • Rare disease research strategy and biomarker mapping

  • Scientific input for regulatory documents and investigator brochures

• Medical Affairs & Scientific Communications

  • KOL engagement strategy and advisory board content

  • Disease state education, slide decks, and scientific messaging

  • Scientific review of promotional and non-promotional materials

Why Partner with Me:

• PhD-level scientific depth and clinical research experience (Duke University)

• Strategic mindset grounded in business training (Executive MBA, USA)

• Proven track record across R&D, regulatory, and medical affairs domains

• Skilled communicator adept at aligning stakeholders across functions

Details of other services-

Medical Writing

• Manuscripts for peer-reviewed journals

• Abstracts, posters, and slide decks for medical congresses

• Medical education and training materials

• Literature reviews and systematic reviews

• Drug monographs and product information documents

Regulatory Writing:

• Clinical Study Reports (CSRs)

• Investigator’s Brochures (IBs)

• Clinical Trial Protocols and Amendments

• Informed Consent Forms (ICFs)

• Briefing Documents (e.g., for FDA, EMA)

• CTD Module 2 and 5 documents

• Risk Management Plans (RMPs)

• Periodic Safety Update Reports (PSURs)

• Regulatory editing and QC review

• Document formatting and compliance with ICH/GCP and journal guidelines

• Reference management using EndNote, Mendeley, etc.

Transcription

Clean English file of a medical transcript from webinar or lecture recorded in different accent:  grammar and scientific accuracy guaranteed.