Clinical Research Associate

📋 Description

• Monitor clinical investigative sites to ensure successful protocol execution, data quality
• Conduct site qualification, initiation, interim monitoring, and study closeout visits for Phase I
• Ensure clinical sites adhere to GCP, ICH guidelines, applicable regulations, monitoring plans
• Proactively identify site issues, develop and communicate corrective actions, and follow through on
• Oversee site personnel activities without direct authority, building effective relationships and
• Maintain regulatory inspection readiness at assigned clinical sites and ensure required

🎯 Requirements

• Appropriate tertiary qualification in a health-related discipline such as medicine, science
• Minimum of 2 years of clinically related monitoring experience, including on-site monitoring of
• Strong knowledge of clinical research practices and relevant therapeutic indications.
• In-depth understanding of regulations governing clinical research, including ICH/GCP guidelines and
• Familiarity with key aspects of clinical study monitoring, including data review, drug
• Strong planning, organizational, and time-management skills, with the ability to manage multiple

🎁 Benefits

• Innovative and collaborative work environment focused on meaningful clinical research.
• Professional development and career growth opportunities.
• Paid time off, including vacation, holidays, personal days, and volunteer days.
• Employee stock purchase opportunities.
• Wellness spending account.
• Flexible health insurance options.