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Medical/scientific/academic writer

3 years experience into medical writing and academic research.Currently associated with a top MNC as Editor for cortellis competitive intelligence.Below are highlights from my work ? Creation and review of the highest quality scientific and medical content across a range of written communications including presentations, publications and digital media ? Drafting/quality check of Module 2 Common Technical Documents like Non-Clinical Overview (Module 2.4), Non-clinical summary (Module 2.6) and supporting IND projects. ? Writing newsletters, writing clinical study protocol, informed consent form, investigators brochure. ? Write and edit clinical study documents. ? Perform independent peer review/ QC of several medical writing documents. ? Authoring, revision and review publications and presentations for peer-reviewed journals and major conferences pertaining to the development of investigational medications and clinical, preclinical and drug development phase molecules. ? Registering and updating radiopharmaceutical and radio-diagnostic drug records in cortellis. Key areas: ? Gene therapy, immuno-oncology, stem cell therapy, radiopharmaceutical and radio-diagnostic. ? To perform literature reviews including the retrieval and analysis of data, study design terms, competitive product pipeline information, epidemiology trends, treatment patterns etc. ? Process clinical trial data (Phase I to IV including observational studies) and abstracting clinical information providing supporting and related information for required analysis.

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$10/hr Ongoing

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3 years experience into medical writing and academic research.Currently associated with a top MNC as Editor for cortellis competitive intelligence.Below are highlights from my work ? Creation and review of the highest quality scientific and medical content across a range of written communications including presentations, publications and digital media ? Drafting/quality check of Module 2 Common Technical Documents like Non-Clinical Overview (Module 2.4), Non-clinical summary (Module 2.6) and supporting IND projects. ? Writing newsletters, writing clinical study protocol, informed consent form, investigators brochure. ? Write and edit clinical study documents. ? Perform independent peer review/ QC of several medical writing documents. ? Authoring, revision and review publications and presentations for peer-reviewed journals and major conferences pertaining to the development of investigational medications and clinical, preclinical and drug development phase molecules. ? Registering and updating radiopharmaceutical and radio-diagnostic drug records in cortellis. Key areas: ? Gene therapy, immuno-oncology, stem cell therapy, radiopharmaceutical and radio-diagnostic. ? To perform literature reviews including the retrieval and analysis of data, study design terms, competitive product pipeline information, epidemiology trends, treatment patterns etc. ? Process clinical trial data (Phase I to IV including observational studies) and abstracting clinical information providing supporting and related information for required analysis.

Skills & Expertise

Academic ConsultingAcademic WritingAnalyticsCommunication SkillsContent WritingData ManagementDesignEditingLikesLiteratureMedicalModule DesignPattern DesignPresentationsPublication ProductionQuality Assurance (QA) And TestingReview WritingRewriting And RevisionsScientificSoftware DevelopmentSummarizingWriting

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