Address
SalaryAbiomed, part of Johnson & Johnson's MedTech, is recruiting for a Sr Statistical Programmer, located in Danvers MA. Remote work options may be considered on a case-by-case basis and if approved by the Company.
The Sr Statistical Programmer will be responsible for providing hands-on data analysis support in clinical project teams. This individual will participate in the design, development, documentation, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data and analysis results for Abiomed studies.
Key Responsibilities:
- Generate and validate tables, listings, and figures (TLF) based on statistical analysis plan (SAP)
- Work with statistician to provide statistical analysis support for publication effort
- Use major statistical programming language to perform data analysis for various needs
- Provide statistical analysis support for post approval studies
- Write specifications and statistical programs to generate analysis datasets and outputs
- Perform data analysis tasks with minimal supervision
- Work with statisticians to develop statistical toolbox for advanced data modelling, tabulation, and visualization
- Participate in reviewing and validating data analysis results
Qualifications
Education:
- Minimum Education of a Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field is required. An MS Degree in Statistics, Mathematics, Computer Science, or related field is preferred
Experience and Skills:
Required:
- 3 years experience with a Master’s degree OR 6 years experience with a Bachelor’s degree is required
- Strong SAS programming skill in producing various types of outputs such as TLFs and datasets
- Extensive statistical programming experience in producing deliverables either on scheduled or adhoc basis
- Experience with producing outputs submitted to the FDA and other regulatory agencies
- Excellent organizational skill to prioritize multiple tasks and goals to ensure timely completion
- Attention to detail and able to adapt to a fast-paced environment
- Ability to work both independently and in a cross-functional team
- Excellent communication skills
Preferred:
- Sufficient knowledge in CDISC and SDTM/ADAM for FDA submission compliance
- Adequate knowledge in clinical trial research methodology, ICH, GCP and regulations
- Experiences in medical device and cardiovascular disease is desirable, but not required
Salary
For U.S. applicants, in accordance with applicable disclosure requirements, the anticipated base pay range for this position is $115,000 to $190,000.
Bonus
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding individual and the corporation’s performance over a calendar/ performance year. Bonuses are awarded at the Company’s discretion on an individual basis.
Benefits
Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans. For additional general information on company benefits, please go to:
https://www.careers.jnj.com/employee-benefits
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Working with Johnson & Johnson can change everything. Including YOU.
#JNJDataScience
