# Site Partner II

**Company**: ICON
**Location**: Mexico City
**Work arrangement**: hybrid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Site-Partner-II--Regulatory-Submissions-_JR161069?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/site-partner-ii-5358d6ca-25c/

## 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 Partner II at ICON, you will support investigator sites with key administrative and operational activities to help ensure clinical trials run smoothly, efficiently, and in compliance with applicable regulations.

**Responsibilities:**

- Support preparation, process and tracking of site level critical documents and/or of site activation tasks required for site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP

- Maintain accurate site information and status updates in clinical trial management systems and trackers

- Assist with site communications, meeting scheduling, and follow-up on outstanding actions

- Help prepare materials for site visits, meetings, and audit or inspection activities

- Ensure site-related documentation is filed correctly to support inspection readiness

- Collaborate with CRAs, Clinical Site Associates, and project teams to resolve basic site queries

**Your Profile:**

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

- Initial experience in clinical research, administration, or a similar regulated environment is preferred

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

- Good communication skills and a customer-focused approach to supporting sites and internal colleagues

- Comfort working with spreadsheets, databases, and standard office software

- Willingness to learn clinical trial processes, GCP principles, and site operations

**Rewards & Benefits:**

- 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

For more fresh new jobs, check out [yubhub.co](https://yubhub.co/).

## Skills

### Required
- clinical research
- administration
- organisational skills
- communication skills
- GCP principles

### Nice to have
- life sciences
- healthcare
- business

---

Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Site-Partner-II--Regulatory-Submissions-_JR161069?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)