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Clinical Research Associate, CRA
Novo NordiskClinical Research Associate at Novo Nordisk managing clinical trial sites in South Africa. Ensuring protocol compliance, data integrity, and the protection of patient safety during trials.
Tech Stack
Tools & technologiesGoogle 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
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringRBQM principlesICH-GCP guidelinesregulatory requirementsclinical trials methodology
Soft Skills
organizational skillstime management skills