- Monitor clinical trials and ensure compliance with regulations, GCP, and SOPs.
- Conduct site qualification, initiation, interim, and closeout visits.
- Train site staff and proactively manage site performance.
Qualifications:
- Health-related degree with clinical research monitoring experience.
- Knowledge of ICH/GCP guidelines and applicable regulations.
- Strong planning, analytical, and communication skills.
- Remote based in Madrid with travel to study sites.
- Dynamic environment with competing projects and deadlines.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, and neuroscience. It is a global biopharmaceutical company committed to integrity, innovation, and transforming lives.
#J-18808-LjbffrClinical Research Associate I (Fully Remote) in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.