Clinical Trial Associate 2/3 – Sponsor Dedicated
Location
Hungary
Posted
1 day ago
Salary
0
Seniority
Mid Level
Job Description
Clinical Trial Associate 2/3 – Sponsor Dedicated
ICON plc
• You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges • Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records • Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements • Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study • Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials • Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success
Job Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Must have working experience prior as a CTA in CRO or Pharma company in clinical research
- Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements
- Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively
- Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management
- Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders
- Willingness to travel as required (approximately 10%)
Benefits
- 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
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• Provide administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records • Assist in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements • Collaborate with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study • Monitor and track trial progress, including managing site communications and ensuring timely delivery of study materials • Build and maintain strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success
• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. • Support the preparation of study-related materials, such as informed consent forms and case report forms. • Work with cross-functional teams to facilitate communication and ensure smooth trial execution. • Contribute to the tracking and reporting of clinical trial metrics and milestones.
• Support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. • Contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. • Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues. • Assist in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations. • Collaborate with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle. • Track site performance metrics, analyzing data, and providing reports to enhance site management efficiency. • Participate in training initiatives and mentoring junior staff to support their development in clinical trial management.
