Clinical Research Liaison
TempusFull Time
Entry Level & New Grad, Junior (1 to 2 years)
Candidates must possess a Graduate/Bachelor's degree in life sciences or a related field, with at least 1+ year of relevant work experience in a pharmaceutical or scientific environment. Foundational knowledge of clinical study delivery processes, including regulations and industry standards, is required, along with strong project management skills and excellent verbal and written English communication. Proficiency in Microsoft Office tools and clinical trial management systems is also necessary.
The Clinical Trial Coordinator will work closely with the Study Manager or Study Delivery Lead on end-to-end operational study delivery activities, ensuring completeness of internal systems and project plans. Responsibilities include collaborating across departments, monitoring study conduct and progress, reviewing key clinical documents, and leading the development of study plans. The role involves facilitating communication, coordinating vendor relationships and study-specific deliverables, managing country-specific activities, and overseeing the delivery of clinical supplies and investigational products. Additionally, the coordinator will ensure the study is inspection ready, manage budget oversight, and track expenses.
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.