Senior/ICF Medical Writing Project Manager Job at Thermo Fisher in Palm Coast

ICF Medical Writing Project Manager

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital, and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. We have a vacancy for an ICF Medical Writing Project Manager based in a number of global locations.

Our Medical Writing team is growing and we are looking for a Senior/ICF Medical Writing Project Manager in multiple locations in the EMEA region.

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.

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!