Sr. Clinical Research Associate

📋 Description

• Independently conduct and document onsite and remote activities, including site monitoring and
• Collaborate with site staff to ensure data consistency and compliance with study requirements
• Monitor, resolve and/or facilitate resolution of data queries and escalate issues
• Coordinate shipment of clinical supplies including investigational product, laboratory supplies
• Ensure site staff training on protocol, study plans, systems and ICH-GCP
• Participate in routine study progress meetings, teleconferences and Investigator's meetings

🎯 Requirements

• 4-6 years of related experience (minimum), 7-9 years preferred
• Honors Bachelor's degree (minimum), Master's degree preferred
• Fluent in written and verbal English
• Health Sciences, Life Sciences, Pharmacy or Nursing degree preferred or Sr.CRA/ACRP Certification
• Experience with Phase I-IV clinical trials preferred
• Thorough knowledge of ICH-GCP and local regulatory requirements

🎁 Benefits

• Annual Bonus target of 8% of annual salary
• Monthly stipend of 400 RON for communication costs
• Monthly cell phone stipend of 50 RON
• One-time expense reimbursement of up to 500 RON for office items
• Mileage reimbursement for travel