Sr Site Activation Specialist- Fsp

SyneosHealth

Site start-up process management
Regulatory submission expertise
Clinical trial contract negotiation
The role is responsible for quality deliverables at the country level with minimal oversight from the SSU Country Manager

Job Summary

  • The role is responsible for quality deliverables at the country level with minimal oversight from the SSU Country Manager.
  • Candidates will act as a liaison between investigational sites and functional leads to oversee site activation end-to-end.
  • Syneos Health offers career development, technical training, and an inclusive culture driven by the purpose of accelerating patient progress.

Matching Summary

The role is responsible for quality deliverables at the country level with minimal oversight from the SSU Country Manager.

Skills & Requirements

Must-have

  • Site Start-Up process management
  • Regulatory submission expertise
  • Clinical trial contract negotiation
  • Country-level regulatory intelligence
  • Trial Master File compliance

Nice-to-have

  • Vendor management experience
  • Mentoring junior team members
  • Data protection guidance skills
  • Continuous improvement mindset
  • Cross-functional collaboration

Key Requirements

  • Experience in Site Start-Up (SSU) operations
  • Knowledge of local regulatory authorities and EC submissions
  • Ability to negotiate investigator contracts and budgets
  • Understanding of clinical trial data protection requirements

Work Rights

Not specified

Tailored Resume

Cover Letter