Focused on delivering precise, compliant medical content as an experienced Medical Editor with GCP?ICH certification.
Aktualisiert am 26.06.2026
Profil
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 26.06.2026
Verfügbar zu: 100%
davon vor Ort: 100%
? AMA/FDA Guidelines
? Copy Editing
? Fact-Checking
? Scientific Documentation
? Microsoft Teams
? Microsoft Word
? Microsoft Excel
Adobe Workfront
Proofreading
? Good Clinical Practice (GCP)
? ICH Guidelines (E6
E8
E3
etc.)
? Data Integrity & ALCOA+ Principles
Data Entry
? Patient Safety & Rights Protection
? SOP adherence/Audit ready documentation habits
? Trial Master File (TMF) Management
? Clinical Trial Documentation
? Veeva Vault
? PowerPoint
English
Native/Bilingual
German
Beginner
Hindi
Native/Bilingual

Einsatzorte

Einsatzorte

Berlin (+50km)
Deutschland, Schweiz, Österreich
möglich

Projekte

Projekte

3 Jahre 11 Monate
2022-07 - 2026-05

Copyedit healthcare content for clarity, accuracy, and compliance

Senior Medical Editor
Senior Medical Editor
  • Copyedit healthcare content for clarity, accuracy, and compliance with AMA and APA style guidelines. 
  • Enhance SEO performance and readability through strategic content optimization. 
  • Recommend substantial edits to improve content quality, structure, and adherence to editorial standards. 
  • Perform rigorous proofreading and quality control to minimize errors across all production stages. 
  • Collaborate with cross-functional editorial teams to develop engaging, audience-focused health content. 
  • Review and proofread assessment/test items throughout the production lifecycle. 
  • Edited 1,000+ manuscripts, consistently delivering high-quality output with zero client complaints. 
WebMD, Mumbai, India
4 Jahre 8 Monate
2017-12 - 2022-07

Supported in drafting and reviewing 1,200+ standard manuscripts annually

Content Reviewer
Content Reviewer
  • Supported BIS scientists in drafting and reviewing 1,200+ standard manuscripts annually. 
  • Copyedited and proofread technical and regulatory documents across multiple BIS departments, ensuring high accuracy and zero client complaints. 
  • Improved document quality, consistency, and compliance across CED, FAD, MED, PCD, and other divisions. 
  • Delivered meticulous editing and proofreading, consistently receiving positive stakeholder feedback. 
  • Collaborated with cross-functional teams to maintain clarity, accuracy, and adherence to established standards. 
BSB Edge, New Delhi, India
1 Jahr 3 Monate
2016-10 - 2017-12

Prepared and proofread draft versions of Indian and international standards

Proofreader and Data Entry Operator
Proofreader and Data Entry Operator
  • Prepared and proofread draft versions of Indian and international standards for gazette publication. 
  • Managed and maintained document repositories to ensure accurate version control and accessibility. 
  • Created and updated editorial and formatting documents in line with organizational guidelines. 
  • Published finalized standards on BIS and the Government of India portals, ensuring accuracy and timely dissemination. 
Bureau of Indian Standards (BIS), New Delhi, India

Aus- und Weiterbildung

Aus- und Weiterbildung

11 Monate
2014-07 - 2015-05

Diploma in Medical Image Processing (MIP)

Banasthali University, Jaipur, India
Banasthali University, Jaipur, India
2 Jahre 11 Monate
2011-07 - 2014-05

Bachelor of Science (Biotechnology)

Kolhan University, Jamshedpur, India
Kolhan University, Jamshedpur, India
2 Jahre 11 Monate
2011-07 - 2014-05

Bachelor of Science (Biotechnology)

Kolhan University, Jamshedpur, India
Kolhan University, Jamshedpur, India

Kompetenzen

Kompetenzen

Top-Skills

? AMA/FDA Guidelines ? Copy Editing ? Fact-Checking ? Scientific Documentation ? Microsoft Teams ? Microsoft Word ? Microsoft Excel Adobe Workfront Proofreading ? Good Clinical Practice (GCP) ? ICH Guidelines (E6 E8 E3 etc.) ? Data Integrity & ALCOA+ Principles Data Entry ? Patient Safety & Rights Protection ? SOP adherence/Audit ready documentation habits ? Trial Master File (TMF) Management ? Clinical Trial Documentation ? Veeva Vault ? PowerPoint

Produkte / Standards / Erfahrungen / Methoden

PROFESSIONAL SUMMARY

Entry?level Clinical Research Coordinator with an M. Sc. in Biotechnology and 7+ years of experience in medical editing, scientific accuracy review, and regulatory?aligned documentation. Skilled in protocol interpretation, data verification, cross?functional communication, and maintaining high?quality study documentation, seeking to transition into clinical operations with a strong foundation in GCP principles, medical terminology, and detail?oriented workflow management. 


SKILLS

  • Proofreading 
  • Copy Editing 
  • Scientific Documentation 
  • Scientific Content Editing 
  • Scientific Quality Control (QC/QA) 
  • Scientific Accuracy Review 
  • Reference Management & Citation Verification 
  • Fact-Checking using Primary Literature 
  • Documentation & Template Management 
  • PowerPoint 
  • Microsoft Word 
  • Microsoft Excel 
  • Workfront 


CLINICAL & SCIENTIFIC SKILLS

  • Good Clinical Practice (GCP)  
  • ICH Guidelines (E6, E8, E3, etc.)   
  • Clinical Trial Documentation 
  • Trial Master File (TMF) Management 
  • Risk-Based Monitoring (RBM)   
  • Data Integrity & ALCOA+ Principles   
  • SOP adherence/Audit-ready documentation habits 
  • Patient Safety & Rights Protection  

Einsatzorte

Einsatzorte

Berlin (+50km)
Deutschland, Schweiz, Österreich
möglich

Projekte

Projekte

3 Jahre 11 Monate
2022-07 - 2026-05

Copyedit healthcare content for clarity, accuracy, and compliance

Senior Medical Editor
Senior Medical Editor
  • Copyedit healthcare content for clarity, accuracy, and compliance with AMA and APA style guidelines. 
  • Enhance SEO performance and readability through strategic content optimization. 
  • Recommend substantial edits to improve content quality, structure, and adherence to editorial standards. 
  • Perform rigorous proofreading and quality control to minimize errors across all production stages. 
  • Collaborate with cross-functional editorial teams to develop engaging, audience-focused health content. 
  • Review and proofread assessment/test items throughout the production lifecycle. 
  • Edited 1,000+ manuscripts, consistently delivering high-quality output with zero client complaints. 
WebMD, Mumbai, India
4 Jahre 8 Monate
2017-12 - 2022-07

Supported in drafting and reviewing 1,200+ standard manuscripts annually

Content Reviewer
Content Reviewer
  • Supported BIS scientists in drafting and reviewing 1,200+ standard manuscripts annually. 
  • Copyedited and proofread technical and regulatory documents across multiple BIS departments, ensuring high accuracy and zero client complaints. 
  • Improved document quality, consistency, and compliance across CED, FAD, MED, PCD, and other divisions. 
  • Delivered meticulous editing and proofreading, consistently receiving positive stakeholder feedback. 
  • Collaborated with cross-functional teams to maintain clarity, accuracy, and adherence to established standards. 
BSB Edge, New Delhi, India
1 Jahr 3 Monate
2016-10 - 2017-12

Prepared and proofread draft versions of Indian and international standards

Proofreader and Data Entry Operator
Proofreader and Data Entry Operator
  • Prepared and proofread draft versions of Indian and international standards for gazette publication. 
  • Managed and maintained document repositories to ensure accurate version control and accessibility. 
  • Created and updated editorial and formatting documents in line with organizational guidelines. 
  • Published finalized standards on BIS and the Government of India portals, ensuring accuracy and timely dissemination. 
Bureau of Indian Standards (BIS), New Delhi, India

Aus- und Weiterbildung

Aus- und Weiterbildung

11 Monate
2014-07 - 2015-05

Diploma in Medical Image Processing (MIP)

Banasthali University, Jaipur, India
Banasthali University, Jaipur, India
2 Jahre 11 Monate
2011-07 - 2014-05

Bachelor of Science (Biotechnology)

Kolhan University, Jamshedpur, India
Kolhan University, Jamshedpur, India
2 Jahre 11 Monate
2011-07 - 2014-05

Bachelor of Science (Biotechnology)

Kolhan University, Jamshedpur, India
Kolhan University, Jamshedpur, India

Kompetenzen

Kompetenzen

Top-Skills

? AMA/FDA Guidelines ? Copy Editing ? Fact-Checking ? Scientific Documentation ? Microsoft Teams ? Microsoft Word ? Microsoft Excel Adobe Workfront Proofreading ? Good Clinical Practice (GCP) ? ICH Guidelines (E6 E8 E3 etc.) ? Data Integrity & ALCOA+ Principles Data Entry ? Patient Safety & Rights Protection ? SOP adherence/Audit ready documentation habits ? Trial Master File (TMF) Management ? Clinical Trial Documentation ? Veeva Vault ? PowerPoint

Produkte / Standards / Erfahrungen / Methoden

PROFESSIONAL SUMMARY

Entry?level Clinical Research Coordinator with an M. Sc. in Biotechnology and 7+ years of experience in medical editing, scientific accuracy review, and regulatory?aligned documentation. Skilled in protocol interpretation, data verification, cross?functional communication, and maintaining high?quality study documentation, seeking to transition into clinical operations with a strong foundation in GCP principles, medical terminology, and detail?oriented workflow management. 


SKILLS

  • Proofreading 
  • Copy Editing 
  • Scientific Documentation 
  • Scientific Content Editing 
  • Scientific Quality Control (QC/QA) 
  • Scientific Accuracy Review 
  • Reference Management & Citation Verification 
  • Fact-Checking using Primary Literature 
  • Documentation & Template Management 
  • PowerPoint 
  • Microsoft Word 
  • Microsoft Excel 
  • Workfront 


CLINICAL & SCIENTIFIC SKILLS

  • Good Clinical Practice (GCP)  
  • ICH Guidelines (E6, E8, E3, etc.)   
  • Clinical Trial Documentation 
  • Trial Master File (TMF) Management 
  • Risk-Based Monitoring (RBM)   
  • Data Integrity & ALCOA+ Principles   
  • SOP adherence/Audit-ready documentation habits 
  • Patient Safety & Rights Protection  

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