Clinical Research Associate, Single Sponsor dedicated in Poland
Core
Performing monitoring and site management work to ensure clinical trial sites conduct studies and report data per protocol and regulations.
Role type
Junior Clinical Research Associate (on-site monitoring)
Builds
Clinical trial data integrity and regulatory compliance for life sciences sponsors
Domain
Life sciences / Clinical research
Deliverable
client delivery
Required skills
GCP and ICH guidelines knowledge, site selection and initiation, subject recruitment planning, CRF completion tracking, data query resolution, Microsoft Office proficiency, Polish (fluent), English (fluent)
Preferred skills
Experience with on-site monitoring clinical trials
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Performing site selection, initiation, monitoring and close-out visits; supporting subject recruitment plan development; administering protocol training to sites; evaluating site practice quality; tracking regulatory submissions and data query resolution
Seniority
Junior, hands-on IC
