Similar Jobs
See allClinical Research Associate II / Senior CRA
Ergomed
Clinical Trials
Regulatory Submissions
Communication
Senior Clinical Research Associate (CRA)
MapLight Therapeutics
US
Clinical Research
GCP
Site Management
Clinical Research Associate
Orca Bio
US
Oncology
Data Management
CTMS
Senior Clinical Research Associate
Precision for Medicine
France
Monitoring
ICH-GCP
Regulatory Submissions
Senior Clinical Trial Associate
Jobgether
US
Clinical Research
GCP
FDA Regulations
Key Responsibilities:
- 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.
Work Environment:
- 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.