Responsibilities:

• Provide coordination support for a team of Medical Writing staff, including supervising Medical Writing staff as needed
• Performs technical and quality control review of regulatory/medical/technical documents prepared by the Medical Writing staff including clinical trial meeting summaries
• Works with assigned Medical Writing Managers and Project Managers to manage timelines, productivity, and quality of deliverables
• Participates in project team and client meetings as required
• Develops and implements standard operating procedures specific to medical writing functions
• Maintains a quality control process for all processes
• Identifies and implements document review and approval processes
• Manages consistency of style and format for regulatory/medical/technical documents
• Develops scope and specific responsibilities with regards to client specific requests/projects
• Contributes to technical proposals and Business Development activities

Requirements:

• Advanced degree in life science/medical field with 5+ years of experience
• Outstanding writing and editing skills
• Advanced knowledge of researching, writing, editing, and reviewing clinical and regulatory documents
• Excellent time management and multi-tasking skills
• Experience in attending and moderating large meetings preferred
• Excellent customer service skills
• Prior supervisory experience a plus
• Proficiency in Microsoft Office

Job Snapshot