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Accountabilities:
- Develop and maintain clinical data listings, reports, and programming solutions to support data review activities.
- Create listing specifications based on user requirements, protocols, EDC databases, and data validation specifications.
- Support the development of reports and listings used for centralized monitoring activities.
Requirements:
- Bachelor’s degree in Science or related discipline; Master’s preferred.
- Minimum 10 years of clinical research experience and at least 5 years of SAS programming experience.
- Strong understanding of clinical trial data, regulatory requirements, and industry standards.
Benefits:
- Fully remote home-based position in India with flexible work schedule.
- Opportunity to contribute to global clinical research programs and mentor junior team members.
- Continuous learning and professional development opportunities in a supportive workplace culture.
Partner Company
A partner company in the clinical research industry supports global clinical research programs through data analysis and programming. The company offers a fully remote, collaborative environment with a focus on continuous learning and improvement.