US Site Activation Specialist for Clinical Trials

7050 INC Research Clinical Services Mexico Limited, S.A. de C.V.; Argentina; Remote; ARS 83,778,000 - 114,242,000; Full time

Job summary

Syneos Health is seeking a Site Activation Specialist (US Experience) to drive end-to-end site activation within country scope and ensure regulatory submissions are prepared and tracked efficiently. The role involves collaboration with CSA, SAM, and PM to manage timelines and document control across trials.

The ideal candidate will have experience in start-up activities, familiarity with TMF requirements, and a proactive approach to problem solving in a dynamic biopharmaceutical setting.

Qualifications

• Experience supporting site activation and regulatory submissions.
• Ability to follow SOPs and maintain training records.
• Track milestone progress and coordinate with cross-functional teams.

Responsibilities

• Manage site activation end-to-end within country/site scope.
• Prepare regulatory submissions and maintain TMF documentation.
• Coordinate with SAM/PM and CSA for project start-up activities.

Skills

Site activation

Project coordination

Regulatory submissions

Tools

SOPs

RA Applications

Job description

Syneos Health is seeking a Site Activation Specialist (US Experience) to drive end-to-end site activation within country scope and ensure regulatory submissions are prepared and tracked efficiently. The role involves collaboration with CSA, SAM, and PM to manage timelines and document control across trials.

The ideal candidate will have experience in start-up activities, familiarity with TMF requirements, and a proactive approach to problem solving in a dynamic biopharmaceutical setting.