Atorus Research India is a leader in clinical trial analytics, renowned for its innovative tools and solutions that enhance data management and biometrics activities. By leveraging automation and advanced technologies, Atorus aims to maximize trial efficiency, ease data interpretation, and enable actionable insights from clinical trial data.
Job Overview
As an Electronic Data Capture (EDC) Programmer, you will play a pivotal role in supporting clinical database creation, deployment, and maintenance. This position is integral to ensuring compliance with Atorus’ and sponsors’ SOPs, Good Clinical Practice (GCP), and ICH Guidelines. The role also involves providing technical support for data collection systems, directly contributing to successful clinical trials.
Key Responsibilities
- Develop, deploy, and maintain clinical databases using Veeva CDMS or Medidata Rave.
- Program eCRFs, rules, and study deployment activities.
- Configure Veeva CDMS, including eCRFs, events, schedules, and EDC tools.
- Understand the Veeva CDMS object hierarchy and post-production change processes.
- Interact with clients to address EDC programming queries and issues.
- Organize and prioritize workloads to meet project deadlines.
- Continuously learn new domains and technologies to enhance technical expertise.
Qualifications and Skills
- Experience: 1–3 years in EDC programming, specifically with Veeva CDMS or Medidata Rave.
- Technical Expertise: Proficiency in eCRF development, rules programming, and study deployment.
- Certification: Veeva Study Builder certification (preferred).
- Communication: Strong ability to collaborate with clients and team members.
- Soft Skills: Enthusiastic learner with excellent organizational and prioritization skills.
