Clinical Research Liaison
TempusFull Time
Entry Level & New Grad, Junior (1 to 2 years)
Candidates should possess a Bachelor's degree or equivalent, with 2-5 years of relevant experience. A strong understanding of contract law principles, including business, intellectual property, and local tax laws, is required. Proficiency in English and the local language, along with strong attention to detail, analytical skills, and the ability to use Microsoft Office Suite, are essential. Familiarity with the pharmaceutical product development process and CRO involvement is also necessary.
The Site Contract Specialist will draft, review, negotiate, and finalize agreements with study sites, ensuring compliance with local processes and company guidelines. This includes negotiating investigator grant budgets and contractual terms within approved parameters, identifying and assessing risks, and recommending resolutions. The role involves coordinating with internal departments to align site startup activities with contractual timelines and achieving target cycle times for site activations.
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.