Senior Medical Writing Project Manager
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Job Description
Senior ICF Medical Writing Project Manager leading compliant Informed Consent Form and clinical research documentation projects. Managing timelines, budgets, quality, and cross-functional delivery for Thermo Fisher Scientific.
Responsibilities:
- Develop project timelines, standards, budgets, and forecasts
- Collaborate with cross-functional teams to meet deliverables
- Monitor timelines and provide status updates
- Identify and resolve client management issues
- Ensure compliance with quality processes
- Lead initiatives involving Informed Consent Forms (ICFs) and other critical clinical research documents
- Deliver high-quality, compliant medical writing project outputs
Requirements:
- Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience
- Experience managing medical writing or clinical projects
- Pharmaceutical/CRO industry experience preferred
- Experience in regulatory and/or plain language medical writing advantageous
- Proven project management skills
- Strong planning and organizational abilities
- Excellent interpersonal and communication skills
- Ability to work independently and under pressure
- Solid project management, budgeting, and forecasting skills
- Effective problem-solving and decision-making abilities
- Proficient in global and regional regulatory guidelines
Benefits:
- Competitive remuneration
- Annual incentive plan bonus
- Healthcare
- Range of employee benefits
- Career and development prospects
- Innovative, forward-thinking organization
- Exciting company culture centered on integrity, intensity, involvement, and innovation
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