# Clinical Trial Associate

**Company**: ICON Strategic Solutions
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Greece-Athens/Clinical-Trial-Associate_JR162800?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As a Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

**Responsibilities**

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges. Key responsibilities include:

- 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.

**Your Profile**

You will have a strong foundation in clinical trial management, with the experience to work independently and guide others. Required qualifications and experience:

- Bachelor's degree in a relevant scientific discipline or healthcare-related field

- Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.

- Strong organisational 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%).

**Rewards & Benefits**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- 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

## Skills

### Required
- clinical trial management
- regulatory requirements
- documentation management
- communication skills
- problem-solving skills

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