Clinical Data Report Programmer (India)

Exciting Opportunity in India!

Bachelor's degree (or equivalent education) in Life Sciences, Computer Science, Statistics, Biostatistics, Data Science, Health Sciences, or a related field.

• Experience: Minimum of 5–7 years' experience in Clinical Data Management report programming within the biopharmaceutical industry or a Contract Research Organization (CRO).
• Minimum of 5–7 years' experience in Clinical Data Management report programming within the biopharmaceutical industry or a Contract Research Organization (CRO).

• High-level English language proficiency.
• Strong understanding of Clinical Data Management principles, workflows, and clinical trial data review processes.
• Extensive knowledge of clinical database structures and Electronic Data Capture (EDC) systems.
• Experience developing and maintaining EDC system reports , clinical data review reports, patient profiles, listings, dashboards, and data cleaning reports.
• Ability to interpret clinical study protocols, edit check specifications, data review plans, and reporting requirements.
• Proficiency in SAS, SQL, Python, R, and JReview .
• Experience working with multiple clinical data sources, external data, and reconciliation datasets.
• Strong understanding of CDISC standards, including SDTM and controlled terminology (preferred).
• Knowledge of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements.
• Strong analytical, problem-solving, and troubleshooting skills.
• Excellent attention to detail with a commitment to data quality, integrity, and accuracy.
• Ability to manage multiple studies and competing priorities simultaneously.
• Strong organizational and time management skills.