Syneos Health

Syneos Health

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13 días
Expira 08/08/2026

Site Activation Specialist I

Site Activation Specialist I

Company Overview

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity and accelerate progress.

Team Collaboration

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience to understand customer needs and shape effective solutions. Join us in a Functional Service Provider partnership or a Full-Service environment, collaborating with passionate problem-solvers.

Why Syneos Health

  • We are passionate about developing our people through career development and a supportive management structure.
  • We foster an inclusive culture where you can authentically be yourself, driven by our purpose to make impactful solutions.
  • We aim to shape the future of healthcare by bringing together smart colleagues from across the world.

Job Responsibilities

  • Provide quality assurance on deliverables at the country level with oversight from the SSU Country Manager.
  • Track submission timelines and milestones, providing justifications for delays and assisting with contingency planning.
  • Monitor financial aspects and ensure procedural compliance regarding training and documentation.
  • Manage essential document packages for site activation, regulatory submissions, and act as a liaison with investigational sites.

Get to Know Syneos Health

In the past 5 years, Syneos Health has been involved with 94% of all Novel FDA Approved Drugs and engaged in over 200 Studies. Learn more about us at syneoshealth.com.

Additional Information

Responsibilities are not exhaustive and may change at the company's discretion. Equivalent experience will be considered, and nothing should be construed as creating an employment contract.

Summary

This role involves activities that lead to the start-up of investigative sites for clinical trials, ensuring compliance with timelines and quality standards.