# SMA I

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Malaysia-Kuala-Lumpur/SMA-I_JR160414?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_70927ad3-7da

## Description

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

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency.

**What You Will Do:**

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include:

- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

- Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.

- Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.

- Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.

- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.

**Your Profile:**

You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience:

- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.

- Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.

- Strong organisational skills and attention to detail, with the ability to manage multiple tasks effectively.

- Basic knowledge of clinical trial processes and regulatory requirements is a plus.

- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.

- Willingness to travel as required (approximately 25%).

**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.

Benefits may vary depending on role and location.

## Skills

### Required
- Good Clinical Practice (GCP)
- clinical trial management
- life sciences
- healthcare administration
- clinical research

### Nice to have
- organisational 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/Malaysia-Kuala-Lumpur/SMA-I_JR160414?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)