Medical Writer- Home based
Overview
Demonstrates ability to use computerized systems (PC-Windows and MS Word). Exhibits excellent written and oral communication and presentation skill. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documentation.
Responsibilities
Contributes to project plan concerning organization and table layout for a specific document.
Ensures that documents meet regulations, and the key messages as defined by the team are clearly and adequately represented.
Review study concepts and edit protocols for consistency, progression, structure, and grammar.
Review statistical analysis plans and incorporate into clinical study reports.
Drive the document preparation process, receive and review primary statistical output, draft and distribute document for review, and compile comments and edits as necessary.
Participate in team and client meetings as requested
Qualifications
Advanced degree in a relevant scientific/clinical/regulatory field preferred
At least 5 years of pharmaceutical industry experience in the clinical/regulatory field
Global regulatory submission experience.
Excellent writing skills.
Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.
Knowledge of current requirements and guidelines applicable to submission documents
Excellent interpersonal and oral communication skills.
Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
Ability to prioritize multiple projects
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
Demonstrates ability to use computerized systems (PC-Windows and MS Word). Exhibits excellent written and oral communication and presentation skill. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documentation.
Responsibilities
Contributes to project plan concerning organization and table layout for a specific document.
Ensures that documents meet regulations, and the key messages as defined by the team are clearly and adequately represented.
Review study concepts and edit protocols for consistency, progression, structure, and grammar.
Review statistical analysis plans and incorporate into clinical study reports.
Drive the document preparation process, receive and review primary statistical output, draft and distribute document for review, and compile comments and edits as necessary.
Participate in team and client meetings as requested
Qualifications
Advanced degree in a relevant scientific/clinical/regulatory field preferred
At least 5 years of pharmaceutical industry experience in the clinical/regulatory field
Global regulatory submission experience.
Excellent writing skills.
Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.
Knowledge of current requirements and guidelines applicable to submission documents
Excellent interpersonal and oral communication skills.
Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
Ability to prioritize multiple projects
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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