Director of Medical Writing overseeing projects and teams related to oncology at Johnson & Johnson. Responsible for strategic decision-making and regulatory document guidance.
Responsibilities
Assume overall accountability for decision-making within the organization or TA.
Proactively identify potential risks and develop strategies to mitigate them.
Recognize and resolve complex problems related to new service offerings and deliverables.
Write or provide guidance on clinical, regulatory, and safety documents.
Represent the MW department with decision-making authority in the R&D organization.
Directly lead or set objectives for team projects and tasks.
Serve as a liaison between team members and senior leadership.
Develop, implement, and drive process improvements and best practices.
Mentor, support, and coach staff at all levels on document planning and content.
Accountable for MW resource management and allocation within their portfolio(s).
Requirements
A university/college degree in a scientific discipline is required.
An advanced degree (eg, Masters, PhD, MD) is preferred.
Minimum of 14 years of relevant pharmaceutical/scientific experience is required.
Minimum of 12 years of relevant clinical/medical writing experience is required.
Minimum of 5 years of people management experience is required.
Experience providing strategic and operational leadership to medical writing teams across all levels.
Expertise in project management and process improvement is required.
Strong decision-making skills, strategic thinking, agility, broad vision is required.
Excellent oral and written communication skills.
Attention to detail.
Expert time management for self, direct reports (if applicable), and teams.
Expert ability to lead and influence by example and stay focused (positive).
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