Clinical Document Specialist

Key Clinical Trial Documents SpecialistDevelops high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).Translates complex scientific data into clear, regulatory compliant documents supporting drug development and approval...

Clinical Publishing Coordinator Job SummaryWe are seeking a highly skilled Clinical Publishing Coordinator to join our team. The successful candidate will be responsible for creating and modifying clinical investigator manuals, requisitions and other relevant materials according to SOW requirements.Key Responsibilities:Create and modify clinical investigator...

Job Summary:We are seeking a highly skilled and detail-oriented Medical Document Reviewer to join our team. As a key member of our medical review process, you will be responsible for reviewing and assessing medical documents, including clinical trial data, safety reports, and regulatory submissions.

Job OpportunityWe are seeking a skilled professional to fill the role of Clinical Outreach Specialist. As a Clinical Outreach Specialist, you will play a vital part in engaging with communities and promoting our services.

Job DescriptionKey Accountabilities- Document Management:- Track, scan, code, and apply naming conventions to documents per the Central File Maintenance Plan (CFMP).- Archive and manage paper documents in the Central Files office.- Conduct photocopying, printing, distribution, and retrieval of documents as required.- Perform basic quality checks to ensure...

Job Title: Clinical Data SpecialistAbout the Role:The Clinical Data Specialist plays a pivotal part in our organization by accurately coding medical records to facilitate efficient data indexing.This key position involves a range of activities, including but not limited to:Coding patient records with precision and speed.Ensuring compliance with established...

About the RoleWe are seeking a skilled Clinical Document Author to join our team.This individual will be responsible for authoring and analyzing clinical trial documents, working with key clinical documents including protocols, informed consent forms, and clinical study reports.The ideal candidate will have experience in clinical research or a related field...

Medical Transcription SpecialistWe are seeking a highly skilled and detail-oriented Medical Transcription Specialist with 3 to 20 years of experience to join our healthcare documentation team.Key Responsibilities:Transcribe medical dictations accurately, interpreting and documenting information into well-structured medical records.Edit and proofread...

Job OverviewDevelop high-quality clinical trial documents, including protocols and study reports.Translate complex scientific data into clear, regulatory compliant documents.Key Responsibilities:Create key clinical trial documents such as protocols, investigator's brochures, informed consent forms, case report forms, and clinical study reports.Communicate...

Unlock the Power of Clinical Research DocumentationDevelop comprehensive clinical trial documents, including protocols and Investigator's Brochures that showcase scientific excellence.Translate complex data into clear, compliant documents supporting drug development and regulatory submissions, ensuring accuracy and precision.Craft compelling abstracts and...