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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.

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