Lead Medical Writer – Remote (Canada)

Parexel; United States; Remote; USD 63.000 - 91.000; Vollzeit

Benefits dieser Stelle

Fully remote from Canada

Global projects and collaboration

Flexible work arrangements

Zusammenfassung

Parexel, a leading global clinical development partner, is seeking a Principal Medical Writer for a fully remote, Canada-based role. You will lead complex regulatory and clinical writing projects, coordinate cross-functional teams, and mentor colleagues to ensure high-quality deliverables across diverse programs.

Join a collaborative, impact-driven team that supports drug development worldwide. Excellent communication, project management, and regulatory writing expertise are essential for

Qualifikationen

• Bachelor’s degree in Life Sciences or related field.
• Strong understanding of clinical research, drug development, and applicable regulatory guidelines.
• Extensive experience preparing CSRs, IBs, and ICFs.
• Demonstrated experience managing complex medical writing projects.
• Knowledge of resource planning and productivity management.
• Proficiency in Microsoft Word; familiarity with SharePoint and Excel.
• Fluency in written and spoken English.

Aufgaben

• Lead clinical and regulatory writing with high scientific accuracy and regulatory compliance.
• Drive project leadership by coordinating multiple writers and cross-functional teams.
• Build trusted relationships with clients and internal partners to align expectations and deliverables.
• Mentor colleagues, share best practices, and drive continuous improvement in processes.

Kenntnisse

Bachelor's degree

Medical writing

Regulatory writing

Project leadership

English fluency

Ausbildung

Bachelor’s degree in Life Sciences or related

Tools

Microsoft Word

SharePoint

Excel

Jobbeschreibung

Parexel, a leading global clinical development partner, is seeking a Principal Medical Writer for a fully remote, Canada-based role. You will lead complex regulatory and clinical writing projects, coordinate cross-functional teams, and mentor colleagues to ensure high-quality deliverables across diverse programs.

Join a collaborative, impact-driven team that supports drug development worldwide. Excellent communication, project management, and regulatory writing expertise are essential for