Position Title:
Stat Programmer Scientist
Location:
Bengaluru, India
Employment Type:
Full Time
Job ID:
R1476381
Job Overview:
At a team, site, or staff level, the Stat Programmer Scientist provides advanced technical expertise to develop process methodologies to meet both internal and external client needs. This role involves planning and coordinating the development of integrated programming solutions across the full spectrum of statistical programming. The individual will offer technical leadership, internal consulting, and collaborate with cross-functional teams to analyze complex client or project requirements.
Key Responsibilities:
Technical Execution:
Plan, coordinate, and implement programming, testing, and documentation of statistical programs for complex studies.
Create statistical tables, listings, figures, analysis datasets, and transfer files for internal and external clients.
Program quality control checks for source data and periodically report data issues.
Specifications & Development:
Interpret complex project-level requirements and translate them into programming specifications.
Provide advanced technical expertise and independently propose project solutions for statistical programming challenges.
Project & Team Leadership:
Act as technical team lead for complex studies or a group of studies.
Communicate directly with internal statisticians, client statisticians, and clinical team members.
Ensure appropriate understanding of project requirements, and monitor and communicate project timelines and deliverables.
Resource Management:
Estimate scope of work and manage resource assignments.
Provide timely updates on project status and adjust/re-negotiate timelines as needed.
Promote the adoption of SOPs, best practices, and established standards.
Training & Mentoring:
Offer training and mentorship to statistical programming team members.
Help build departmental expertise and consistency in programming practices.
Required Qualifications:
Education:
Bachelor's Degree in Mathematics, Computer Science, Statistics, or a related field and 10 years of relevant experience required
OR Master’s Degree in the above disciplines and 9 years of relevant experience preferred
Equivalent combination of education, training, and experience will be considered
Experience & Skills:
Minimum 7+ years of relevant experience in statistical programming within clinical trials
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language
Excellent understanding of statistics and the clinical drug development process
Strong organizational, interpersonal, and leadership skills
Precision and strong attention to detail
High-level problem-solving capabilities and mathematical aptitude
Advanced knowledge of data standards such as CDISC, ADaM, and SDTM
Ability to work collaboratively with colleagues, managers, and clients
About the Company:
IQVIA is a global leader in clinical research services, healthcare analytics, and technology solutions for the life sciences industry. Through intelligent connections, IQVIA supports innovation and accelerates the development of life-changing treatments to improve health outcomes worldwide.
Application Link:
Apply Now at IQVIA Careers
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