Clinical Research Associate
Abarca HealthFull Time
Junior (1 to 2 years)
Candidates should possess a Bachelor’s degree and demonstrate a minimum of 2 years of experience in clinical research coordination, with a preference for experience within the pharmaceutical or biotechnology industry. Strong organizational skills and attention to detail are essential, along with the ability to work effectively both independently and as part of a team. Familiarity with clinical trial processes and regulatory guidelines is highly desirable.
The Clinical Trial Coordinator will provide administrative and technical support to the Project Team, ensuring audit readiness by reviewing files and adhering to SOPs. They will support site activation activities, develop the critical path for site activations, represent the CRG personnel, and act as a buddy during onboarding. The role involves coordinating trial activities, performing file reviews, ensuring timely processing of documents, providing system support, analyzing study metrics, assisting with investigator site file preparation, and supporting scheduling and regulatory document review. Additionally, they may conduct on-site feasibility visits and contribute to RBM activities.
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.