Medical Content Specialist

As a key member of the medical writing team, we seek an experienced and skilled Sr. Medical Editor to join our team.

• Maintain familiarity with FDA, EU, and other relevant guidelines and industry standards to ensure documents meet or exceed sponsor and regulatory requirements and guidance.
• Represent the editorial group in Medical Writing, on study teams, and in cross-departmental project teams as needed.
• Monitor timelines and budgets for assigned projects and update the Lead Medical Writer, Project Manager, and/or direct supervisor (as appropriate) if deliverables are at risk.
• Provide technical support and expertise as appropriate. Conduct training of medical editing staff and function as a mentor. Advise medical writers, medical editors, and study teams on data integrity review, compilation, publishing, and editorial standards. Provide 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.
• Serve as a member of the medical writing team for projects with medical writing deliverables. Provide feedback to the lead medical writer on progress of document editorial process.
• Copyedit assigned documents, applying correct grammar, punctuation, spelling, and style following American Medical Association (AMA) or various custom style guidelines as well as established medical writing internal checklists and best practices.
• Perform data integrity review of assigned documents to ensure accuracy.
• Contribute to the development of process improvement tools and the development or revision of internal policies and procedures affecting editorial work.
• Manage assigned projects according to medical writing standard operating procedures and client standards, on time and on budget.
• May compile and publish medical writing deliverables.

Requirements:

• Bachelor's degree in 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 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.

Benefits:

This role offers an exciting opportunity to contribute your expertise and collaborate with a talented team.

What We Offer:

• A dynamic and supportive work environment.
• Ongoing opportunities for professional growth and development.
• A competitive compensation package.

How to Apply:

We encourage you to apply if you have the necessary skills and qualifications.