# SMA II

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/SMA-II_JR163974-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/sma-ii-45430e12-695/

## 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 II at ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

**What You Will Do:**

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:

- Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.

- Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.

- Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.

- Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency.

- Participating in training initiatives and mentoring junior staff to support their development 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.

- Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines.

- Strong organisational and project management skills, with the ability to handle multiple priorities and deadlines.

- Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards.

- Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams.

- This role is office-based for the first four months, followed by a hybrid working model.

**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.

**Inclusion and Accessibility**

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

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## Skills

### Required
- Good Clinical Practice (GCP)
- clinical research
- site management
- monitoring
- project management
- analytical skills
- communication skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/SMA-II_JR163974-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)