Senior Medical Editor
hace 3 semanas
We are seeking a highly skilled Senior Medical Editor to join our team at Pharmiweb. As a key member of our Medical Writing team, you will be responsible for maintaining the highest standards of quality and accuracy in our regulatory documents.
Key Responsibilities:
- Maintains familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure that documents meet or exceed sponsor and regulatory requirements and guidance.
- Represents the editorial group in Medical Writing, on study teams, and in cross-departmental project teams as needed.
- Monitors timelines and budgets for assigned projects and updates the Lead Medical Writer, Project Manager, and/or direct supervisor (as appropriate) if deliverables are at risk.
- Provides technical support and expertise as appropriate.
- Conducts training of medical editing staff and functions as a mentor.
- Advises medical writers, medical editors, and study teams on data integrity review, compilation, publishing, and editorial standards.
- Provides training to members of the global Medical Writing team in aspects relative to their roles.
- Project lead for deliverables of assigned complex and/or large medical writing projects, including but not limited to scheduling and leading internal project-specific team meetings, organizing project-specific requirements, and ensuring that all information is distributed to the editorial team and implemented within the deliverable.
Requirements:
- Bachelor's degree (preferred) in the life sciences, clinical sciences, or English/journalism; or copyediting, data integrity review, and/or relevant publishing experience.
- Significant relevant publishing experience using Adobe Acrobat or other appropriate markup language preferred; ISIToolbox experience preferred.
- Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint).
- Excellent attention to detail, including strong copyediting, data integrity review, accuracy, problem solving, organizational, interpersonal, presentation, project management, and team-oriented skills.
- Excellent grammatical and communication skills, both written and oral.
- Extensive familiarity with the AMA style guide strongly preferred.
- Ability to work with minimal supervision on multiple assignments with set deadlines.
- Ability to work independently as well as part of a team and keep others informed of the progress and status of projects.
- Adaptable to changes in work duties, responsibilities, and requirements.
- Knowledge of FDA and EU requirements, ICH regulations and ISO standards as applicable to regulatory documents preferred.
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