Clinical Research Associate
Abarca HealthFull Time
Junior (1 to 2 years)
Candidates should possess a Bachelor's degree in a life sciences field or a Registered Nursing certification, with experience comparable to over two years as a clinical research monitor. A valid driver's license is also required, and equivalent combinations of education, training, and experience may be considered.
The SR CRA I will monitor investigator sites using a risk-based approach, applying root cause analysis and critical thinking to identify and resolve compliance issues. Responsibilities include ensuring data accuracy through reviews, assessing investigational products, documenting observations, escalating deficiencies, and maintaining communication with sites. The role also involves tracking trial status, updating study systems, participating in investigator meetings, identifying potential investigators, initiating clinical trial sites, ensuring document completeness, and contributing to project teams and process improvements.
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.