Senior ICF Medical Writing Project Manager

Work Schedule

Environmental Conditions

Job Description

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 Europe (locations listed).

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.

Education

• Prefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience.

Experience

• Experience managing medical writing or clinical projects.
• Pharmaceutical/CRO industry experience preferred.
• Advantageous to have experience in regulatory and/or plain language medical writing.

Knowledge, Skills, Abilities

• Solid project management, budgeting, and forecasting skills.
• Effective problem-solving and decision-making abilities.
• Proficient in global and regional regulatory guidelines.

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. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!