We have a current opportunity for a Sr Manager/AD Statistical Programming - R on a permanent basis. The position will be based in Massachusetts or Illinois. For further information about this position please apply.
Job Title: Sr Manager/Associate Director, Statistical Programming
Job Type: Full-Time
We're a dynamic and innovative pharmaceutical company dedicated to improving patient outcomes through cutting-edge research and development. We are committed to fostering a collaborative and inclusive work environment where every team member can thrive.
Job Summary: We are seeking a highly skilled and motivated Sr Manager/Associate Director of Statistical Programming with extensive experience in R and SAS to join our growing team. The successful candidate will lead and oversee statistical programming activities for clinical trials, ensuring the highest standards of data integrity and analysis.
Key Responsibilities:
- Lead and manage a team of statistical programmers, providing mentorship and guidance.
- Develop and implement statistical programming strategies and plans for clinical trials.
- Collaborate with biostatisticians, data managers, and clinical teams to ensure accurate and timely delivery of statistical outputs.
- Create, validate, and maintain complex statistical programs using R and SAS.
- Ensure compliance with regulatory requirements and industry standards.
- Review and approve programming deliverables, including datasets, tables, listings, and figures (TLFs).
- Participate in the development of standard operating procedures (SOPs) and best practices.
- Provide technical expertise and support for ad-hoc analyses and data requests.
- Drive strategy and resourcing in conjunction with departmental needs and initiatives
- Stay current with industry trends and advancements in statistical programming and R and SAS.
Qualifications:
- Master's in Statistics, Biostatistics, Computer Science, or a related field.
- Minimum of 8 years of experience in statistical programming within the pharmaceutical or biotechnology industry.
- Proficiency in R programming and SAS is required.
- Strong understanding of clinical trial design, data management, and regulatory requirements.
- Excellent leadership and team management skills.
- Strong problem-solving abilities and attention to detail.
- Effective communication and interpersonal skills.
- Ability to work collaboratively in a fast-paced, dynamic environment.
Benefits:
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Retirement savings plan with company match.
- Generous paid time off and holiday schedule.
- Professional development opportunities.
- Collaborative and inclusive work culture.