Global Site Activation Lead

Syneos Health, Inc.; Morrisville (NC); On-site; USD 80,000 - 140,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (medical, dental, and/

401k match

Employee Stock Purchase Plan

Bonuses / commissions eligibility

Flexible PTO and sick time

Job summary

Syneos Health, Inc. is seeking a Sr Site Activation Manager to lead site activation and start-up activities for global clinical trials.

You will oversee regulatory submissions and serve as the main point of contact for site start-up, coordinating with sponsors, sites, vendors, and cross-functional teams. The role requires proactive risk mitigation, knowledge of regulatory requirements, and the ability to manage multiple studies in a fast-paced global environment.

Responsibilities

• Lead and manage site activation and start-up activities for global clinical trials, ensuring milestones and timelines are met.
• Oversee regulatory, ethics/IRB, and site activation submissions across multiple countries and regions.
• Serve as the primary point of contact for site start-up activities, partnering with sponsors, sites, vendors, and cross-functional teams.
• Drive issue resolution and proactively identify and mitigate risks that may impact study timelines.
• Provide strategic oversight and guidance on country-specific regulatory requirements and start-up processes.
• Track start-up metrics, study deliverables, and activation performance, ensuring compliance with study objectives.
• Support and mentor junior team members and contribute to process improvement initiatives.
• Ensure compliance with GCP, applicable regulations, and company SOPs.
• Collaborate with Project Management and Clinical Operations teams to support successful study execution.
• Manage multiple studies and priorities in a fast-paced global environment.

Job description

Syneos Health, Inc. is seeking a Sr Site Activation Manager to lead site activation and start-up activities for global clinical trials.

You will oversee regulatory submissions and serve as the main point of contact for site start-up, coordinating with sponsors, sites, vendors, and cross-functional teams. The role requires proactive risk mitigation, knowledge of regulatory requirements, and the ability to manage multiple studies in a fast-paced global environment.