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Lead Statistical Programmer
hace 2 meses
Position Overview:
As a Lead Statistical Programmer, you will leverage your extensive technical knowledge to establish and refine methodologies that align with both internal and external client requirements. You will orchestrate the creation of comprehensive programming solutions that cater to a wide array of statistical programming demands.
Key Responsibilities:
- Oversee and execute the following for intricate studies:
- Development, validation, and documentation of statistical programs designed for generating statistical tables, figures, and listings.
- Creation of analysis datasets (derived datasets) and transfer files for various stakeholders.
- Conduct quality control checks on source data and systematically report any data discrepancies.
- Translate project-level requirements into programming specifications for complex studies.
- Provide advanced technical insights in collaboration with both internal and external clients, delivering project solutions to Statistical Programming teams.
- Assume project responsibilities as the technical team lead for individual complex studies or groups of studies.
- Engage directly with internal statisticians and clinical team members to ensure a clear understanding of project requirements and timelines.
- Estimate programming workloads, manage resource allocations, communicate project progress, and negotiate timelines for deliverables.
- Offer training and mentorship to Statistical Programming team members.
Qualifications:
- Minimum of 5 years of experience in Statistical Programming within the Life Sciences sector.
- BSc or MSc degree in Biostatistics or a related discipline.
- Proficient in SAS Base, with a solid understanding of SAS Graph and SAS Macros.
- Capability to implement advanced statistical methods as specified by Biostatisticians.
- Strong knowledge of CDISC standards (SDTM and ADaM).
- Comprehensive understanding of relational database principles.
- Exceptional application development skills.
- Deep familiarity with clinical trial data, including hands-on experience in data manipulation, analysis, and reporting.
- Ability to manage multiple projects while effectively planning, organizing, and prioritizing tasks.
- Experience as a technical team lead, directly interacting with clients and coordinating team efforts.
- Thorough knowledge of relevant clinical research regulatory standards, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Why IQVIA?
At IQVIA, we are committed to fostering a culture of innovation and collaboration. Our diverse global team is dedicated to utilizing advanced analytics, cutting-edge technologies, and extensive healthcare expertise to drive meaningful advancements in health worldwide. We offer:
- Global exposure across various therapeutic areas.
- A collaborative and supportive team environment.
- Access to innovative in-house technology.
- Excellent opportunities for career development and progression.
- A focus on work-life balance and employee well-being.
Unleash your potential with IQVIA, where your skills can make a significant impact in the healthcare landscape.
