Clinical Research Associate (Multiple Roles)
On-site
Core
Site-facing Clinical Research Associate ensuring high-quality execution and compliance for Phase I–IV clinical trials.
Role type
Senior IC Clinical Research Associate
Builds
Clinical trial data integrity and patient safety across multiple study sites
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, Good Clinical Practice (GCP), regulatory compliance, risk assessment, site relationship management, training delivery
Preferred skills
Drug development process knowledge, site management experience
Technologies
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
Seniority
Mid-level, hands-on IC