Clinical Research Associate
Abarca Health- Full Time
- Junior (1 to 2 years)
Candidates should possess a degree in Life Sciences or equivalent experience, with at least one to two years of independent on-site monitoring experience, and a strong understanding of Good Clinical Practice (GCP). They must also have fluency in both English and French languages, hold a full French driving license, and be comfortable with nationwide travel.
The Junior Clinical Research Associate will work in partnership with a single sponsor, typically allocated to one to two protocols within areas like Oncology, Neurology, Immunology, and/or Diabetes, managing approximately 10 sites and conducting on-site monitoring between 6 and 8 days per month. Responsibilities include site management and monitoring activities in France, collaborating with sites to adapt and track subject recruitment plans, creating and maintaining monitoring visit reports and action plans, and providing protocol and study training to assigned sites. The role also involves becoming part of the team and contributing to the sponsor’s pipelines, utilizing Risk Based Monitoring to reduce travel 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.