Experienced CRA - Sweden
Core
Perform site monitoring visits and manage clinical trial sites to ensure adherence to study protocols, regulations, and sponsor requirements.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical/biotech studies
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
Site monitoring (selection, initiation, close-out), GCP compliance, subject recruitment tracking, protocol administration, regulatory submission tracking, CRF management, data query resolution, TMF/ISF documentation, site financial management
Preferred skills
Scientific or healthcare degree background, therapeutic area knowledge
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Conduct site monitoring visits, drive subject recruitment plans, administer protocol training, evaluate site quality and regulatory adherence, track regulatory submissions and enrollment, manage site documentation and TMF/ISF files, generate visit reports and action plans, support site financial management
Seniority
Mid-level, hands-on IC
