Job Description Summary
Responsible for configuring and managing the Central Monitoring Platform by translating study requirements into >
Job Description
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
Skills Desired
Clinical Trials, Computer Programming, Data Analysis, Programming Languages, Reporting, Statistical Analysis
