Expert Clinical Programmer

Key Responsibilities

• Implement solutions for RBQM, data review and cleaning, as defined in data quality plans and enable the detection of data quality insights.
• Manage configuration of system to support data ingestion, transformation and provisioning required standard and study specific outputs ( e.g. KRIs, QTLs ). Use SAS or Python programming skills while developing required outputs.
• Troubleshoot and resolve routine technical issues related to build, transformations, reports, and visualizations.
• Support post‑production changes by performing impact analysis and helping implement approved change requests.
• Participate in key study milestones such as database go‑lives, dry runs, interim snapshots, and database locks.
• Support system upgrades and validations, including impact assessments and execution of validation activities.
• Develop and maintain study documentation, ensuring accuracy, completeness, and compliance with standards.
• Collaborate with internal teams and vendors, act as subject matter expertise while continuously sharing knowledge within the team.

Essential Requirement

• Minimum 6 years of experience in clinical review and report programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry
• Strong knowledge of any programming languages (SAS, Python, R etc.)
• Knowledge of Data Review and/or Business Intelligence tools (such as Central monitoring platform)
• Understanding of clinical data management systems and/or relational databases as applied to clinical trials
• Ability to translate technical concepts for non- technical users in the areas of central monitoring platform design and visualization development
• Strong verbal and written communication skills to work with our global partners and customers
• Understanding of Drug Development Process, ICH- GCP, CDISC standards and Health Authority guidelines and regulations