Site Specialist I (Ciudad de México)

Site Specialist I (Ciudad de México)

02 sep
|
ICON San Antonio
|
Ciudad de México

02 sep

ICON San Antonio

Ciudad de México

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Site Specialist I 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.

What You Will Do

You will contribute to site management and operations activities, taking responsibility for your deliverables and working collaboratively.

Key Responsibilities Include

Supporting the collection, review, and tracking of essential site documents in accordance with study requirements and SOPs.
Maintaining accurate site information and status updates in clinical trial management systems and trackers.
Assisting with site communications, meeting scheduling, and follow-up on outstanding actions.
Helping prepare materials for site visits, meetings, and audit or inspection activities.




Ensuring site-related documentation is filed correctly to support inspection readiness.
Collaborating with CRAs, Clinical Site Associates, and project teams to resolve basic site queries.

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 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, G

📌 Site Specialist I (Ciudad de México)
🏢 ICON San Antonio
📍 Ciudad de México

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