R&d - Cso - Clinical Operations Study Lead - Bj

Sanofi

Not specified; not specified; not specified
Not specified
Gcp and ich guidelines knowledge
Cross-functional team leadership
Study budget management and forecasting
Sanofi is seeking a Clinical Operations Study Lead (COSL) responsible for managing clinical studies and ensuring their successful execution while adhering to the highest quality standards. The ideal candidate will have significant experience in clinical operations, strong project management skills, and a collaborative mindset to lead cross-functional teams

Job Summary

  • The Clinical Operations Study Lead is accountable for the end-to-end execution of clinical trials ensuring delivery within timelines, budget, and quality standards.
  • This role requires leading a cross-functional Core Study Team to implement operational plans while leveraging digital tools and AI for operational excellence.
  • Candidates must possess significant experience in clinical operations with strong project leadership skills to manage complex studies in a matrixed environment.

Matching Summary

Match Score: 85

Sanofi is seeking a Clinical Operations Study Lead (COSL) responsible for managing clinical studies and ensuring their successful execution while adhering to the highest quality standards. The ideal candidate will have significant experience in clinical operations, strong project management skills, and a collaborative mindset to lead cross-functional teams.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • GCP and ICH guidelines knowledge
  • Cross-functional team leadership
  • Study budget management and forecasting
  • Regulatory compliance and audit preparation
  • Risk identification and mitigation strategies

Nice-to-have

  • Digitalization and AI innovation experience
  • Lean process improvement skills
  • Strong influencing and negotiation abilities
  • Agile response to study changes
  • Project Management Professional certification

Key Requirements

  • Master's or Bachelor's degree in scientific discipline
  • Significant experience managing clinical studies
  • Solid knowledge of FDA and EMA regulations
  • Strong project management and leadership skills

Work Rights

Not specified

Tailored Resume

Cover Letter