Document Review Specialist - Belgium

Summarized Purpose

The Document Review Specialist is responsible for performing quality reviews and editing clinical documents, regulatory submissions, medical/scientific publications, and other related documents.

Essential FunctionsReviews highly technical documents of all types created within or outside of the company to ensure quality standard that meets or exceeds client's expectations.Verifies scientific logic and clarity of the document by verifying data in tables against source documents, checking for consistency according to current regulatory standards and guidelines.Performs detailed QC review checks of clinical and regulatory documents, tables, publications, annual reports, literature summaries, submission sections, and internal documents.Proofreads or substantively edits documents to correct and streamline grammar, spelling, style, and format.

Verifies that document content is consistent with internal, client, and related authority guidelines.Formats, styles, and troubleshoots functionality and presentation of documents and templates.Assists writers or other team members with supportive tasks -- tracking documents -- as requested.Assists with literature searches, reference management, bibliographies, and libraries.Education

Previous experience working in a CRO or Biopharma company.

College degree or 2 years of education in a related field.3 years of editing related job history

Summarized Purpose

The Document Review Specialist is responsible for performing quality reviews and editing clinical documents, regulatory submissions, medical/scientific publications, and other related documents.

Essential FunctionsReviews highly technical documents of all types created within or outside of the company to ensure quality standard that meets or exceeds client's expectations.Verifies scientific logic and clarity of the document by verifying data in tables against source documents, checking for consistency according to current regulatory standards and guidelines.Performs detailed QC review checks of clinical and regulatory documents, tables, publications, annual reports, literature summaries, submission sections, and internal documents.Proofreads or substantively edits documents to correct and streamline grammar, spelling, style, and format.

Verifies that document content is consistent with internal, client, and related authority guidelines.Formats, styles, and troubleshoots functionality and presentation of documents and templates.Assists writers or other team members with supportive tasks -- tracking documents -- as requested.Assists with literature searches, reference management, bibliographies, and libraries.Education

Previous experience working in a CRO or Biopharma company.

College degree or 2 years of education in a related field.3 years of editing related job history

Knowledge, Skills and AbilitiesMS Office (Word, Excel)Knowledge of other computer software and programs where applicableExcellent communication and organizational skillsDetail orientedAbility to handle multiple tasks and deadlinesAbility to prioritize efficientlyWork Environment Requirements

PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner Able to work upright and stationary and/or standing for typical working hours Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments Able to use and learn standard office equipment and technology with proficiency May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments Able to perform successfully under pressure while prioritizing and handling multiple projects or activities

Knowledge, Skills and AbilitiesMS Office (Word, Excel)Knowledge of other computer software and programs where applicableExcellent communication and organizational skillsDetail orientedAbility to handle multiple tasks and deadlinesAbility to prioritize efficientlyWork Environment Requirements

PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner Able to work upright and stationary and/or standing for typical working hours Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments Able to use and learn standard office equipment and technology with proficiency May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments Able to perform successfully under pressure while prioritizing and handling multiple projects or activities