Profile Details

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USD 65 /hr

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Hire Dr. Tatiana M.

USD 65 /hr

Medical writer with 14+ years of experience in clinical research.

Profile Summary

Medical writer specializing in clinical protocol development, informed consent form (ICF) creation, case report form (CRF) design, investigator-initiated proposals, and regulatory submission documentation. With a solid background in the healthcare and pharmaceutical industries, I bring a comprehensive understanding of regulatory standards and compliance requirements. My meticulous attention to detail, coupled with a strong grasp of scientific principles, ensures the delivery of high-quality, accurate, and compliant documents tailored to client specifications. Dedicated to facilitating the smooth progression of clinical trials and research initiatives, I collaborate closely with stakeholders to produce compelling and effective materials that meet the highest industry standards.

Subject Matter Expertise

• ★ Clinical Trial Documentation
• ★ Clinical Trial Protocol Writing
• ☆ Regulatory Writing
• ☆ Medical Writing
• ☆ Technical & Scientific Writing
• ☆ Experimental Protocols
• ☆ SOP & Protocol Writing

Services

• Writing

Writing Clinical Trial Documentation, Medical Writing

Work Experience

Founder/Consultant

VirtuoMark

January 2024 - Present

Manager, External Research

Amgen

July 2018 - April 2024

Lead Clinical Research Coordinator

Stanford University School of Medicine

August 2014 - July 2018

Clinical Research Coordinator

San Francisco Clinical Research Center (SFCRC)

April 2010 - August 2014

Education

Doctor of Medicine (MD)

Pavlov First Saint Petersburg State Medical University

September 2001 - June 2009

Certifications

• ACRP-Certified Professional (ACRP-CP)

  Association of Clinical Research Professionals (ACRP)

  https://www.credly.com/badges/f2284b01-6c5e-4dcf-a2db-1f2e61a1eab2

  January 2024 - January 2024