Senior Clinical Research Associate

Novartis

Multiple Locations
On-site
Ich/gcp compliance
Site monitoring activities
Clinical trial execution
The Senior Clinical Research Associate (sCRA) position at Novartis entails overseeing clinical trial sites to ensure compliance with protocols and regulations while maintaining data integrity and patient safety. The role requires extensive monitoring experience and a proactive approach to risk management, with a focus on building partnerships with investigational sites. ###

Job Summary

  • The Senior Clinical Research Associate plays a pivotal site-facing role, responsible for ensuring high-quality, compliant, and timely execution of clinical trials.
  • The sCRA independently manages complex clinical trial sites across Phase I–IV studies, conducting on‑site and remote monitoring activities in line with ICH/GCP, local regulations, and Novartis SOPs.
  • Proactively identify site risks, issues, and deviations; drive timely mitigation and resolution.

Matching Summary

Match Score: 85

The Senior Clinical Research Associate (sCRA) position at Novartis entails overseeing clinical trial sites to ensure compliance with protocols and regulations while maintaining data integrity and patient safety. The role requires extensive monitoring experience and a proactive approach to risk management, with a focus on building partnerships with investigational sites. ###

Skills & Requirements

Must-have

  • ICH/GCP compliance
  • site monitoring activities
  • clinical trial execution
  • patient safety
  • data integrity

Nice-to-have

  • strong site partnerships
  • effective risk management
  • audit and inspection readiness
  • global cross-functional teams

Key Requirements

  • Minimum 4 years of pharmaceutical or clinical research experience
  • Degree in a scientific or healthcare discipline
  • Proficient English and local country language
  • Willingness to travel extensively

Work Rights

Not specified

Tailored Resume

Cover Letter