[Remote] Senior Clinical Data Scientist
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