Company Overview
[$COMPANY_OVERVIEW]
Role Overview
We are looking for a highly skilled Director of Statistical Programming to lead our statistical programming team, ensuring the development and implementation of efficient programming solutions that support our clinical trials and research initiatives. This role will involve collaborating with cross-functional teams to drive data analysis and reporting strategies, while mentoring and guiding a team of statistical programmers.
Responsibilities
- Lead and manage a team of statistical programmers, providing technical guidance and fostering professional development
- Oversee the design and implementation of statistical programming processes for clinical trials, ensuring compliance with regulatory standards
- Collaborate with biostatisticians, data managers, and clinical researchers to develop analysis plans and statistical methodologies
- Review and validate programming deliverables, ensuring accuracy and adherence to project timelines
- Establish best practices for statistical programming and data management, driving continuous improvement initiatives
- Engage in strategic planning to align statistical programming activities with organizational goals
Required and Preferred Qualifications
Required:
- Master's degree in Statistics, Biostatistics, Mathematics, or a related field
- 8+ years of experience in statistical programming within a clinical research environment
- Proven track record of leadership experience, managing statistical programming teams
- Expertise in SAS programming and strong understanding of statistical methodologies
Preferred:
- PhD in a relevant field
- Experience with other programming languages such as R or Python
- Familiarity with regulatory submissions and compliance standards
- Experience in therapeutic areas such as oncology or rare diseases
Technical Skills and Relevant Technologies
- Deep knowledge of statistical programming languages and tools, particularly SAS
- Experience with data visualization tools and reporting systems
- Proficiency in managing large datasets and ensuring data integrity
- Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems
Soft Skills and Cultural Fit
- Strong leadership and mentorship capabilities, with a focus on team development
- Excellent communication skills, both verbal and written, with the ability to convey complex data and statistical concepts
- Proactive problem-solving abilities, with a track record of navigating complex challenges
- Ability to work collaboratively across disciplines and influence decision-making
- Commitment to fostering a diverse and inclusive work environment
Benefits and Perks
Annual salary range: [$SALARY_RANGE]
Additional benefits may include:
- Equity options
- Comprehensive health, dental, and vision insurance
- Retirement savings plan with employer matching
- Generous paid time off policy
- Professional development and continuing education stipends
Equal Opportunity Statement
[$COMPANY_NAME] is committed to diversity and inclusion in the workplace. We are proud to be an Equal Opportunity Employer and encourage applications from all qualified individuals without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sexual orientation, or any other basis protected by applicable law.
Location
A successful candidate will be expected to work from the office at least 3 days a week.
