Travel Clinical Research Associate
Abarca Health- Full Time
- Junior (1 to 2 years)
Candidates should possess a Bachelor’s degree in a scientific discipline, such as Biology, Chemistry, or a related field, and have at least 2 years of experience in clinical trial monitoring or site management. Strong knowledge of ICH-GCP guidelines, applicable regulations, and SOPs is essential, along with experience in risk-based monitoring and root cause analysis.
The CRA (Level II) will monitor investigator sites using a risk-based approach, conducting on-site and remote visits to assess protocol and regulatory compliance. They will manage required documentation, ensure data accuracy through reviews, escalate deficiencies, and participate in investigator meetings. Additionally, the CRA will identify potential investigators, initiate clinical trial sites, conduct file reviews, provide status updates, and facilitate communication between sites, the client company, and the PPD project team, ensuring adherence to protocol and regulatory obligations.
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.