Senior Manager, Statistical Programming

This is a fully remote position, open to applicants in India.

📋 Description

• Lead and manage a global team of Statistical Programmers.

• Oversee and coordinate statistical programming tasks across various clinical development initiatives.

• Supervise the creation and evaluation of SDTM datasets, ADaM datasets, Tables, Listings, and Figures (TLFs).

• Ensure that study work is adequately resourced, completed on schedule, within budget, and meets client expectations.

• Provide ongoing feedback, coaching, mentoring, and development support to team members.

• Engage in performance management and evaluation of new team members.

• Develop best practices, controlled documents, templates, reusable text, and other relevant work products.

• Identify departmental challenges and collaborate with senior leadership to address them.

• Act as a senior reviewer and offer support for Statistical Programming tasks.

• Lead or assist with client deliverables for large, complex, or high-priority projects.

• Represent the Statistical Programming team to internal senior leadership and external organizations, including during audits, bid defenses, and conferences.

• Assist the Director of Biostatistics with corporate goals, departmental development, industry trends, and related matters.

• Lead special projects and initiatives aimed at enhancing departmental efficiency, profitability, and operational excellence.

• Establish team goals and expectations while supporting recruitment strategies.

• Manage financial aspects of projects for studies supervised by direct reports.

• Plan and coordinate statistical programming for regulatory submission integration efforts.

• Consult with internal teams on statistical programming for clinical trials across various therapeutic areas.

• Assist with resource forecasts, planning, metrics, and KPIs.

⛳️ Requirements

• Bachelor’s degree or higher in mathematics, statistics, biostatistics, computer science, or a related field.

• More than 10 years of experience in Statistical Programming.

• Proficiency in SAS and R.

• Experience in a CRO setting is preferred.

• Familiarity with industry standards and best practices.

• Ability to manage statistical programming projects, including quality control, budgets, timelines, and resource allocation.

• Capability to support regulatory submission integration work.

• Ability to provide consultation on statistical programming for clinical trials.

• Proficiency in supporting resource forecasting, planning, metrics, and KPIs.

🏝️ Benefits

• Opportunity for remote work.

• Emphasis on work-life balance.

• Opportunities for career growth and development.

• Collaborative environment with an international team.

• Access to coaching, mentoring, and development support.

• Continuous learning opportunities.