# Site Specialist II (Study Start Up Associate II)

**Company**: ICON
**Location**: Taipei, Taiwan
**Work arrangement**: hybrid
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Taiwan-Taipei/Site-Specialist-II_JR162382?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/site-specialist-ii-study-start-up-associate-ii-77463987-7b8/

## Description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.

**Responsibilities**

You will take responsibility for site management and operations deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include:

- Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.

- Acting as an operational liaison for site staff on documentation, systems, and process-related questions.

- Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.

- Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits.

- Identifying opportunities to streamline site workflows and contributing to process improvement initiatives.

- Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.

**Your Profile**

You will bring relevant site management and operations experience, along with the following qualifications and skills. Required qualifications and experience:

- Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience.

- Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare.

- Good understanding of clinical trial processes, GCP, and site documentation requirements.

- Strong organisational and problem-solving skills, with the ability to manage multiple sites and priorities.

- Excellent communication and interpersonal skills, with a proactive, service-focused mindset.

- Comfort working independently while collaborating effectively with cross-functional teams.

**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

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## Skills

### Required
- life sciences
- healthcare
- business
- clinical trial processes
- GCP
- site documentation requirements
- organisational skills
- problem-solving skills
- communication skills
- interpersonal skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Taiwan-Taipei/Site-Specialist-II_JR162382?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)