Travel Clinical Research Associate
Abarca Health- Full Time
- Junior (1 to 2 years)
Candidates should possess a university degree in a scientific discipline or healthcare field, and experience in the pharmaceutical industry or clinical trials environment. Strong computer skills, including MS Office, are required, along with excellent command of Dutch, French, and English languages. The ability to establish and maintain effective working relationships, combined with organizational, time management, and problem-solving skills, is also necessary.
The Clinical Research Associate will perform site monitoring visits, conduct training to sites, manage subject recruitment plans, evaluate site practices, track regulatory submissions and approvals, and ensure proper documentation is maintained in the TMF and ISF. They will also collaborate with study team members, support the start-up phase of studies, and potentially manage site financial aspects according to clinical trial agreements. Additionally, the CRA will generate visit reports, submit follow-up letters, and resolve data queries, while adapting and driving recruitment plans in line with project needs.
Advanced analytics and clinical research services
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.