Clinical Research Associate
Abarca HealthFull Time
Junior (1 to 2 years)
Candidates should possess a High/Secondary school diploma or equivalent, with a Bachelor's degree or equivalent experience preferred. A minimum of 0 to 1 year of relevant experience is required, along with strong organizational skills, attention to detail, and the ability to analyze project-specific data. Proficiency in MS Office and clinical trial database systems is essential, as are excellent communication, interpersonal, and negotiation skills, with the ability to work independently and manage risk.
The Clinical Trial Coordinator will provide administrative and technical support to the Project Team, ensuring audit readiness and supporting site activation activities. Responsibilities include coordinating and completing trial activities, performing file reviews, maintaining system databases, processing documents, analyzing study metrics, and assisting with Investigator Site File and Pharmacy binder materials. The role also involves contributing to the development of global strategic feasibility processes and standard methodologies.
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.