Site Management Associate

• Support the management and monitoring of clinical trial sites
• Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
• Support monitoring activities at clinical trial sites and resolve site-related issues
• Assist in preparing and reviewing regulatory documents
• Collaborate with cross-functional teams throughout the study lifecycle
• Track site performance metrics, analyze data, and provide reports
• Participate in training initiatives and mentor junior staff

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
• Experience in clinical research as a CTA or Global CTA with a solid understanding of clinical trial processes and GCP guidelines
• Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines
• Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards
• Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams
• Legal right to work in Romania

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways