CRA / Sr CRA (Dual Posting)
Core
Site-facing Clinical Research Associate ensuring high-quality execution and compliance for Phase I–IV clinical trials.
Role type
Sr IC Clinical Research Associate
Builds
Clinical trial data integrity and patient safety across multiple study sites
Domain
Life Sciences / Clinical Research
Required skills
Clinical trial monitoring, GCP compliance, regulatory standards knowledge, risk assessment, site relationship management, data integrity management, study closeout, amendment training
Preferred skills
Drug development process understanding, field monitoring experience
Technologies
Clinical Trial Management Systems (CTMS), Clinical Study Reports
Responsibilities
Conduct site initiation visits, perform on-site and remote monitoring, assess site performance and mitigate risks, lead site closeout activities, deliver training on protocols and amendments, build partnerships with clinical trial sites
Seniority
Senior, hands-on IC