Clinical Trial Associate
Location
Poland
Posted
4 days ago
Salary
0
Seniority
Mid Level
Job Description
Clinical Trial Associate
ICON plc
• 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.
Job Requirements
- Bachelor's degree in a scientific or healthcare-related field
- Prior experience or strong interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Excellent organizational and communication skills
- Ability to work collaboratively in a fast-paced environment with attention to detail.
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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• 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.
