Offer summary
Qualifications:
Bachelor’s degree in relevant science discipline preferred, Experience in programming environments like SAS, EDC, SQL, Knowledge of ICH-GCP and regulatory guidelines, Strong understanding of clinical research processes, Proficiency with Software Development Life Cycle methodologies.
Key responsabilities:
- Provide technical expertise for clinical trials
- Set up and maintain electronic data capture systems
- Lead database setup and ensure quality standards
- Interact with sponsors on programming issues
- Participate in creating process standards and documentation