- argenx
- Ghent, Belgium (Remote)
- Full-time
Clinical Editor in Medical Writing
- argenx
Ghent, Belgium
Full-time
Published:
- argenx
Ghent, Belgium
Full-time
Published:
To support the expansion of the Clinical Editing team, we are currently looking for a clinical editor, who will be responsible for ensuring the accuracy of content in clinical and regulatory documents prepared by Medical Writing.
Please note that we are looking to fill in this position on a consultancy basis.
This position reports into the the Global Head of Clinical Editing.
ROLES AND RESPONSIBILITIES:
SKILLS AND COMPETENCIES:
EDUCATION, EXPERIENCE, AND QUALIFICATIONS:
Please include a cover letter with your application that details your motivation for applying to this position.
Keywords: Document Reviewer, Document QC, Document Quality Control, Medical Documentation Review, Quality Control Reviewer, QC Specialist.
Please note that we are looking to fill in this position on a consultancy basis.
This position reports into the the Global Head of Clinical Editing.
ROLES AND RESPONSIBILITIES:
- Responsible for performing quality reviews and editing clinical documents, regulatory submissions, and other related documents;
- Performs detailed data accuracy reviews and fact-checks statements in clinical and regulatory documents, tables, literature summaries, and other internal documents;
- Substantively edits and proofreads 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;
- Communicates with medical writers and other team members to ensure the accuracy of documents;
- Responsible for inspection-readiness of medical writing activities.
SKILLS AND COMPETENCIES:
- Excellent language skills (reading, writing, editing, team communication);
- Ability to interpret clinical data and literature;
- Ability to follow instructions and apply resourceful insight to problem-solving;
- Ability to communicate with professionals from a variety of backgrounds;
- Knowledge of AMA Manual of Style, other style guides, and any guidelines related to assigned projects;
- Expertise in Microsoft Word, including advanced formatting, styles, cross-referencing, bookmarks, and other related skills;
- Fluent in English;
- Expertise in Microsoft Word and understanding of Acrobat/PDF software;
- Experience with Veeva, SharePoint, PerfectIt, and StartingPoint is a plus.
EDUCATION, EXPERIENCE, AND QUALIFICATIONS:
- College degree or 2+ years of education in related field;
- At least 3 years of related experience in document review or medical editing.
Please include a cover letter with your application that details your motivation for applying to this position.
Keywords: Document Reviewer, Document QC, Document Quality Control, Medical Documentation Review, Quality Control Reviewer, QC Specialist.
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