Clinical Research Associate
Abarca HealthFull Time
Junior (1 to 2 years)
Candidates should possess a high school diploma or equivalent, with a Bachelor's degree preferred. A minimum of 0-1 year of relevant experience is required, and an equivalency of education, training, and experience may be considered. Strong organizational skills, attention to detail, and the ability to manage multiple tasks efficiently are essential, along with demonstrated analytical skills for project data and systems.
The Clinical Trial Coordinator will provide administrative and technical support to the Project Team, ensuring audit readiness by reviewing files on schedule according to organizational guidelines. Responsibilities include coordinating and completing trial activities, performing file reviews, ensuring tasks are completed on time and within budget, and communicating project risks. The role involves maintaining study documentation and systems, providing system support (Activate & eTMF), supporting RBM activities, performing administrative tasks such as document processing and reviews, and assisting with scheduling meetings. Additionally, the coordinator will review and track regulatory documents, transmit documents to IRBs/IECs, analyze study metrics, reconcile findings, maintain vendor trackers, and assist with the distribution of site materials and translation coordination.
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.