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Intern - Statistical Programmer/Analyst

ClinChoice Internship Medical Bengaluru / Bangalore, Karnataka, India N/A Posted 26/5/2026

About the Role

Job Title: Intern - Statistical Programming Employment Type: Internship Location: Bengaluru, India About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, vaccine, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, quality-as-a-service, medical affairs, toxicology, and technology solutions to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis. Our global delivery network has expanded to centers and satellite offices in the United States, Canada, the United Kingdom, Italy, Poland, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally. We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision. Primary Responsibilities: This role reports to the Associate Manager, Statistical Programming, and above Successfully complete the clinical programming training program within the agreed time and successfully complete the test conducted after the training program. Also, demonstrate a good understanding in the new project assignments. Effectively ask questions during the training program. Complete all training assignments on time with high quality. Proactively communicate to seniors and seek help to complete the tasks with the first time right (FTR) approach. Produces statistical analysis using SAS/R according to relevant standard operating procedures. Ensuring compliance to SOPs Programming according to specifications Delivers the assigned tasks and projects within agreed timelines and quality standards. Developing SAS Programs for the statistical analysis of study data (low complexity studies), including tables, listings, and figures Program according to CDISC SDTM Communicating effectively with the internal project team. Collaborate closely with the study/working group. Reporting issues to the Project or Study leads or Supervisors in an appropriate time frame. Responsible for continuous development of own skills according to Individual development plan. Actively participate in knowledge-sharing meetings, ask questions, and share feedback to improve the process or standards of the programming continuously. Conduct other administrative and departmental activities as required. Secondary Responsibilities: Behavioral Competencies and Skills Professional Trustworthy Ability to effectively prioritize. Quality focused Personable Attitude Willingness to learn. Team Player Committed, persistent, and accountable. Result Driven

Skills Required

Pharmaceutical

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