Principal Medical Writer
AbbottFull Time
Expert & Leadership (9+ years)
Candidates must possess a BS/BA in a scientific field with 5 years of experience, or an advanced degree with 3 years of experience. Proven project management skills, strong planning and organizational abilities, excellent interpersonal and communication skills, and the ability to work independently and under pressure are required. Pharmaceutical/CRO industry experience is preferred, and experience in regulatory and/or plain language medical writing is advantageous. Solid project management, budgeting, and forecasting skills, effective problem-solving and decision-making abilities, and proficiency in global and regional regulatory guidelines are essential.
The Senior ICF Medical Writing Project Manager will lead initiatives to develop and deliver high-quality, compliant Informed Consent Forms and other critical documents. Responsibilities include developing project timelines, standards, budgets, and forecasts; collaborating with cross-functional teams to meet deliverables; monitoring timelines and providing status updates; identifying and resolving client management issues; and ensuring compliance with quality processes. This role may involve occasional travel to client sites.
Provides life sciences products and services
Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.