Senior ICF Medical Writing Project Manager

Thermo Fisher Scientific • Morrisville, NC

1d • Onsite

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 Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

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.
• Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Number of Employees: 5,001-10,000 employees