Study Delivery Specialist – Unblinded

• Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues
• Assist in preparing and reviewing regulatory documents, ensuring site activities comply with GCP and applicable regulations
• Collaborate with cross-functional teams to facilitate communication and support for trial sites throughout the study lifecycle
• Track site performance metrics, analyze data, and provide reports to enhance site management efficiency
• Participate in training initiatives and mentor junior staff to support their development in clinical trial management
• Contribute to clinical research activities and take responsibility for deliverables

• Master degree in Pharmacy (mandatory)
• Experience in clinical research, site management, or monitoring, 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 Poland

• 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