Remote Country Operations Associate I (Israel)

United States Digital Space LLC; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

Syneos Health in Israel is seeking a Sponsor dedicated Country Operations Associate I to join our Clinical Solutions team remotely. You will support site startup, regulatory submissions, and TMF processes, collaborating with clinical teams, investigators, CROs, and vendors to ensure study milestones are met.

Ideal candidates have 2–5 years of site activation or clinical operations experience, a life sciences degree, and strong organizational and communication skills.

Qualifications

• 2–5 years of site activation, clinical trial support, or clinical operations experience.
• BS/BA in life sciences or related discipline is preferred.

Responsibilities

• Provides operational support across the full site lifecycle: Start-Up, Conduct, and Close-Out.
• Acts as a key contact between clinical teams, investigator sites, CROs, and external partners.
• Supports Regulatory Authority submissions and associated documentation.
• Prepares and maintains Investigator Initiation Packages and essential study documents.
• Performs document management activities in PTMF, eISF, CTMS, and document exchange systems.
• Supports site contracting and budget processes, including momentum tracking and execution status.
• Maintains study trackers, timelines, and task status to ensure visibility of risks and progress.
• Reviews study and site files for completeness and supports TMF/eISF reconciliation activities.
• Contributes to quality, inspection readiness, compliance, and continuous improvement initiatives.

Skills

Site activation

Clinical operations

Regulatory submissions

Communication skills

Education

BS/BA in life sciences

Tools

PTMF

eISF

CTMS

Job description

Syneos Health in Israel is seeking a Sponsor dedicated Country Operations Associate I to join our Clinical Solutions team remotely. You will support site startup, regulatory submissions, and TMF processes, collaborating with clinical teams, investigators, CROs, and vendors to ensure study milestones are met.

Ideal candidates have 2–5 years of site activation or clinical operations experience, a life sciences degree, and strong organizational and communication skills.