Note: The job is a remote job and is open to candidates in USA. Planet Pharma is seeking a Senior Clinical Data Scientist to support clinical development programs. The individual will leverage advanced data science techniques to drive insights, improve data quality, and support operational decision-making across clinical trials.

Responsibilities

• Develop and maintain analytics solutions using Python, SQL, R, and/or SAS
• Analyze clinical and operational datasets to identify trends, risks, anomalies, and opportunities for improvement
• Create dashboards, visualizations, and reports using Power BI, Tableau, or similar business intelligence tools
• Design and support data integration and data pipeline activities across clinical systems and data sources
• Perform data validation, reconciliation, and quality assessments to ensure data integrity
• Collaborate with Clinical Operations, Data Management, Biostatistics, and Technology stakeholders to deliver data-driven solutions
• Translate business requirements into scalable analytical and technical solutions
• Present findings and recommendations to cross-functional teams and leadership
• Support continuous improvement initiatives related to clinical data, analytics, and reporting processes

Skills

• Bachelor's degree in Data Science, Statistics, Mathematics, Computer Science, Information Systems, Biostatistics, or a related field
• 5+ years of experience in clinical data science, clinical analytics, data management, or a related discipline
• Advanced programming skills in Python and SQL
• Experience with R and/or SAS
• Strong understanding of clinical trial data and clinical research processes
• Experience building dashboards and visualizations using Power BI, Tableau, or similar platforms
• Experience working with clinical systems such as Medidata Rave, Oracle, Veeva, CTMS, EDC, or similar technologies
• Strong analytical, problem-solving, and communication skills
• Ability to work effectively with both technical and non-technical stakeholders
• Experience with Risk-Based Quality Management (RBQM) or clinical risk analytics
• Experience with statistical monitoring, risk indicators, and data quality metrics
• Familiarity with clinical analytics platforms such as Medidata Detect, CluePoints, or similar tools
• Knowledge of GCP, ICH guidelines, and clinical trial regulations
• Experience supporting pharmaceutical, biotechnology, medical device, or CRO organizations

Benefits

• Remote opportunity
• Initial 12-month engagement with potential for extension

Company Overview

Company H1B Sponsorship