FSP Associate Director Medical Writing
- Writing types
- Regulatory
- Seniority
- Lead or manager
About the role
Responsibilities
- Manage a Medical Writing group: workload, resources, staff allocation, recruitment, training and performance
- Monitor spending against the departmental budget and manage to the allocation
- Oversee projects led by direct reports and act as first escalation point for project risks
- Assist business development in securing new clients and pricing Medical Writing projects
- Build relationships with other departments and promote new departmental processes and standards
- Handle complex client management issues and prepare complex documents with senior review
Requirements
- Bachelor's degree in a science-related field
- 10+ years of relevant experience, including 5+ years of management responsibility
- Proven leadership and people management skills
- Project management, forecasting and budgeting knowledge
- Knowledge of global medical writing and regulatory requirements for clinical trials
- Excellent communication, negotiation and presentation skills
Preferred Qualifications
- Advanced degree (PharmD, PhD, Masters)
About the Company
- Thermo Fisher Scientific is the world leader in serving science, with annual revenue above $40 billion.
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