The Senior Clinical Data Manager will perform ongoing data review to ensure the accuracy, completeness, and consistency of clinical trial data. They will also collaborate with cross-functional teams to resolve discrepancies and manage database lock activities.
The Associate Director provides technical leadership and mentorship to statistical programmers while managing complex epidemiological and real-world evidence projects. They are responsible for developing robust analytical solutions, ensuring high-quality programming standards, and collaborating with cross-functional teams to support evidence generation.
Lead statistical activities for clinical trials independently, from protocol design to reporting results. Collaborate with cross-functional stakeholders and oversee internal programming or CRO contributions to ensure regulatory compliance.
The Vice President of FSP Operations will lead and scale the India-based Functional Service Provider organization while driving operational excellence and financial performance. This role involves acting as an executive sponsor for strategic client partnerships and fostering a high-performing, collaborative culture across multiple functions.
The role involves leading multiple projects, including systematic literature reviews, while managing client communications and project operations. Additionally, the consultant provides senior-level methodological guidance to junior team members and supports business development activities.
The Principal Leader provides strategic and technical expertise in health economics to optimize pricing, reimbursement, and market access. They are responsible for leading projects, managing client relationships, and mentoring a team of health economists to ensure high-quality deliverables.
The QC Specialist is responsible for planning, executing, and documenting testing activities for EDC systems to ensure they meet specifications and regulatory requirements. They collaborate with cross-functional teams to validate eCRF functionality, manage test documentation, and support system updates prior to study deployment.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while generating and validating SDTM and ADaM datasets. They will also serve as a lead on projects, ensuring high-quality output and effective communication with cross-functional teams and clients.
The Principal Data Scientist will integrate diverse biomedical data sources to develop machine learning models and signal processing methods for clinical research. They are responsible for building scalable data pipelines and ensuring high-quality, reproducible insights from complex high-frequency datasets.
The Senior Biostatistician will provide statistical support for clinical studies, including protocol development, sample size calculations, and the creation of statistical analysis plans. They will also perform statistical analyses, interpret results, and prepare clinical study reports while ensuring compliance with FDA regulations.
The Principal Statistical Programmer will independently manage clinical trial reporting activities, including generating SDTM and ADaM datasets and complex statistical outputs. They will also oversee CRO programming deliverables to ensure high-quality, consistent data summaries that meet regulatory and project timelines.
The role involves preparing programming scripts to generate NONMEM analysis datasets and managing e-submission packages for PK/PD modeling. You will also provide guidance to junior team members and collaborate with cross-functional departments to ensure data quality and process efficiency.
The role involves preparing programming scripts to generate NONMEM analysis datasets and managing e-submission packages for PK/PD modeling. You will also provide guidance to junior team members and collaborate with cross-functional departments to ensure data quality and process efficiency.
Lead statistical activities for clinical trials from protocol design to reporting while collaborating with cross-functional teams. Provide oversight for internal programming and CRO contributions while utilizing advanced statistical methods and machine learning to derive actionable insights.
The Principal Statistical Programmer will independently manage clinical trial reporting activities, including the generation of SDTM and ADaM datasets and complex statistical outputs. They will also oversee CRO programming deliverables and ensure compliance with FDA regulations and clinical development standards.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while ensuring compliance with CDISC standards. They will also lead project tasks, generate submission documents, and collaborate with cross-functional teams to meet project deadlines.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while generating and validating SDTM and ADaM datasets. They will also communicate with cross-functional teams and clients to manage project specifications and submission documentation.
The Principal Statistical Programmer provides technical and project management leadership for SAS programs and clinical trial data analysis. They ensure compliance with regulatory standards and oversee the production of SDTM and ADaM datasets for electronic submissions.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while generating and validating SDTM and ADaM datasets. They will also lead project tasks, communicate with cross-functional teams, and ensure high-quality submission deliverables.
The Senior Biostatistician will provide statistical support for clinical trials, including protocol development, sample size calculations, and the creation of statistical analysis plans. They will also perform statistical analyses, interpret results, and prepare clinical study reports for regulatory submissions.
Program, analyze, and report clinical trial safety and efficacy data using SAS, including generating and validating SDTM and ADaM datasets and tables, listings, and figures. Support or lead clinical studies, prepare submission documents, produce ad-hoc reports, and coordinate with client and cross-functional teams on specifications, status, and issues.
Lead or support clinical data management study activities, CRO oversight, and delivery timelines while coordinating with client stakeholders and cross-functional teams to ensure high-quality, timely data deliverables. Manage vendor budgets and risks, maintain operational processes and inspection-ready records, and contribute to regulatory readiness, governance, and continuous improvement.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials using SAS while ensuring compliance with CDISC standards. They will also generate and validate datasets, tables, listings, and figures, and support submission documentation for regulatory purposes.
