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Novo Nordisk

Clinical Research Associate, CRA

Novo Nordisk

. Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits .

Posted 4/21/2026full-timeSandton • 🇿🇦 South AfricaJuniorMid-LevelWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Oversee and manage assigned clinical trial sites, conducting on-site and remote monitoring visits
  • Drive the implementation of RBQM principles for high-quality execution of clinical trial activities
  • Collaborate with site staff and cross-functional teams for efficient clinical trial execution

Requirements

What you’ll need
  • Bachelor’s degree in Life Sciences or related field
  • At least 4 years’ experience in clinical trial monitoring or relevant pharmaceutical industry/CRO role
  • Strong understanding and knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trials methodology
  • Proficiency in digital tools, including electronic data capture (EDC) systems, CTMS, eTMF, and other clinical trial software
  • Strong organizational and time management skills

Benefits

Comp & perks
  • Opportunities to learn and develop
  • Flexibility to travel as required

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical trial monitoringRBQM principlesICH-GCP guidelinesregulatory requirementsclinical trials methodology
Soft Skills
organizational skillstime management skills