Senior Clinical Research Associate (Remote)

Responsibilities

• Lead assigned sites as the primary point of contact throughout study delivery
• Build strong relationships to ensure site performance, quality, and milestone achievement
• Manage Phase I to Phase IV trials per monitoring plans and company procedures
• Conduct site initiation visits and deliver ongoing training for site personnel
• Perform remote and on-site monitoring to ensure compliance and patient safety
• Identify risks, resolve issues, and escalate concerns as needed
• Collaborate with cross-functional teams to drive efficient study execution

Qualifications

• Minimum of three years of clinical site monitoring experience
• Bachelor's degree in science, healthcare, or related field
• Strong understanding of clinical research and drug development processes
• Knowledge of ICH/GCP and European regulatory requirements
• Ability to manage multiple priorities and work independently
• Strong site management, communication, and problem-solving skills
• Fluency in written and spoken Czech/Slovak and English

Benefits

• Comprehensive benefits package including health, life, and disability benefits
• 401(k) plan with company contribution and match
• Generous time off package including vacation and personal days
• Opportunity for annual equity awards