# Taiwan-FSP-(Senior) Clinical Research Associate-Client office based with flexible WFH

**Company**: ICON Strategic Solutions
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Taiwan-Taipei/XMLNAME--Senior--Clinical-Research-Associate_JR162123?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f66d9b58-776

## Description

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

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

**Responsibilities**

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:

- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

**Your Profile**

You will have a strong foundation in clinical trial monitoring, 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 as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

- Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.

- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

- Willingness to travel as required (approximately 60%)

**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
- Good Clinical Practice (GCP)
- clinical trial monitoring
- data integrity
- site management
- stakeholder management

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Taiwan-Taipei/XMLNAME--Senior--Clinical-Research-Associate_JR162123?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)