Clinical Research Associate
3 mesi fa
**Job Description**:
The role is accountable for performance and compliance for assigned protocols and sites in a
country.
Under the oversight of the CRA manager the person ensures compliance of study conduct with
ICH/GCP and country regulations, policies and procedures, quality standards and
adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study,
taking overall responsibility of allocated sites.
Actively develops and expands the territory for clinical research, finding and developing new
sites.
Participates in internal meetings and workstreams as SME for monitoring processes and
systems.
**Search Firm Representatives Please Read Carefully**
**Employee Status**:
Regular
**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Requisition ID**:R252377
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