Senior ICF Medical Writing Project Manager
About The Position
Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety. We have a vacancy for a Senior ICF Medical Writing Project Manager based in the United States. Discover Impactful Work: Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance. A day in the Life: 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. Keys to Success: Proven project management skills. Strong planning and organizational abilities. Excellent interpersonal and communication skills. Ability to work independently and under pressure. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Requirements
- Proven project management skills.
- Strong planning and organizational abilities.
- Excellent interpersonal and communication skills.
- Ability to work independently and under pressure.
- 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.
- Solid project management, budgeting, and forecasting skills.
- Effective problem-solving and decision-making abilities.
- Proficient in global and regional regulatory guidelines.
Nice To Haves
- Pharmaceutical/CRO industry experience preferred.
- Advantageous to have experience in regulatory and/or plain language medical writing.
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.
Benefits
- We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Number of Employees
5,001-10,000 employees
