Principal Medical Writer
AlconFull Time
Expert & Leadership (9+ years)
Candidates should possess a Bachelor's degree in a scientific field with at least 5 years of experience, or an advanced degree with 3 years of experience. Proven project management skills, strong planning and organizational abilities, and excellent interpersonal and communication skills are essential. The role requires the ability to work independently and under pressure, with experience managing medical writing or clinical projects, preferably in the pharmaceutical/CRO industry. Knowledge of global and regional regulatory guidelines is also required.
The Senior ICF Medical Writing Project Manager will lead initiatives to develop Informed Consent Forms (ICFs) and other critical documents, ensuring quality and compliance. Responsibilities include developing project timelines, standards, budgets, and forecasts. The role involves collaborating with cross-functional teams to meet deliverables, monitoring timelines, providing status updates, and identifying and resolving client management issues. Ensuring compliance with quality processes is also a key duty.
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.