Senior Medical Writer (FSP)

Thermo Fisher Scientific • Morrisville, NC

1d • Onsite

About The Position

At Thermo Fisher Scientific, you will 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. Summarized Purpose: We are seeking a talented and experienced Senior Medical Writer to join our team in NA. The SMW will support our FSP business; experience in EU CTR and early development would be preferred. The Senior Medical Writer will be responsible for developing high-quality clinical and regulatory documents, ensuring they meet all regulatory requirements and company standards.

Requirements

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred.
• 5+ years regulatory writing experience.
• Experience working in the pharmaceutical/CRO industry required.
• Experience in managing and directing complex medical writing projects required.
• Excellent organizational and program management skills
• Proven leadership skills to manage and mentor a team of medical writers.
• Extensive knowledge of regulatory guidelines and drug development processes
• Strong interpersonal and communication skills to build and maintain effective working relationships with colleagues and stakeholders
• Understanding of quality control processes to ensure compliance with regulatory requirements and internal standards
• Self-motivated and adaptable
• Excellent judgment; high degree of independence in decision making and problem solving

Nice To Haves

• Experience in EU CTR and early development would be preferred.

Responsibilities

• Write and edit clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.
• Collaborate with cross-functional teams to gather necessary information and ensure the accuracy and completeness of documents.
• Ensure documents align with regulatory guidelines, company standards, and industry best practices.
• Provide input on document content, structure, and presentation.
• Review and provide feedback on documents prepared by other team members.
• Manage timelines and deliverables for assigned projects.
• Stay current with industry trends, guidelines, and regulatory requirements.

Benefits

• award-winning learning and development programme
• competitive salary
• extensive benefits package based around the health and well-being of our employees
• flexible working culture
• work-life balance

What This Job Offers

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