Offer summary
Qualifications:
1+ year of experience in CSV for clinical trial software, Working knowledge of software development cycle (SDLC), Knowledge of GCP Guidance like 21 CFR Part 11, Expert in Microsoft Word and Excel.Key responsabilities:
- Participate in RTSM requirement gathering sessions
- Collaborate with teams to define clear validation requirements
- Develop and maintain CSV deliverables and test scripts
- Manage validation testing cycles and resolve issues