Category

Medical Writing

Job Type

Full-Time

Education

Bachelor's Degree

Travel

None

Job Description

• Provides coordination support and oversight for a team of Medical Writing Associates, including supervising staff.
• Performs technical and quality control review of documents prepared by the Medical Writing Associates staff including clinical research-related meeting summaries.
• Works with assigned Medical Writing staff, Project Managers, and Task Managers to manage timelines, productivity, and quality of deliverables.
• Participates in project team and client meetings as required.
• Develops and implements standard operating procedures, work instructions, and other tools specific to medical writing associate functions.
• Maintains quality control processes for all procedures including document review and approval processes, consistency of style and format of documents, tracking of timelines, etc.
• Develops scope and specific responsibilities with regards to client specific requests/projects in accordance with project management best practices.
• Contributes to technical proposals and Business Development activities.

Job Requirements

• 5 years experience in life science/medical field.
• Outstanding writing and editing skills.
• Experience in coordinating and overseeing meeting support activities as well as attending and moderating large meetings.
• Experience in project management and/or supervising and mentoring staff preferred.
• Excellent time management and multi-tasking skills.
• Excellent customer service skills.
• Proficiency in Microsoft Office.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.