Overview
On Site
Contract - W2
Skills
Biostatistics
Data Management
FOCUS
Analytical Skill
Knowledge Sharing
Research
Innovation
Process Improvement
Quality Assurance
SAS/MACROS
Workflow
Management
Collaboration
SAS
CDISC
SDTM
Pharmaceutics
Communication
Statistics
Mathematics
Computer Science
Life Sciences
R
S-PLUS
Python
VBA
C++
Publications
DICE
Job Details
Be Part of a High-Performing Team
This role supports a leading organization within the pharmaceutical and biotech sector known for its commitment to advancing clinical development and applying rigorous data standards across global studies. The team operates in a technically sophisticated environment and collaborates closely with biostatistics, clinical operations, and data management. Their work is driven by scientific excellence, efficient processes, and a strong focus on producing reliable, submission-ready outputs. This position is ideal for someone who thrives in an analytical, quality-focused, and fast-paced setting.
What's In Store For You
How You Will Make an Impact
Do you bring proven success in advanced statistical programming?
Required Skills & Experience
Preferred Qualifications
#dice
This role supports a leading organization within the pharmaceutical and biotech sector known for its commitment to advancing clinical development and applying rigorous data standards across global studies. The team operates in a technically sophisticated environment and collaborates closely with biostatistics, clinical operations, and data management. Their work is driven by scientific excellence, efficient processes, and a strong focus on producing reliable, submission-ready outputs. This position is ideal for someone who thrives in an analytical, quality-focused, and fast-paced setting.
What's In Store For You
- An opportunity to play a key role in supporting complex clinical programs.
- A collaborative on-site environment that values knowledge sharing and technical mastery.
- Exposure to impactful project work tied directly to ongoing research and regulatory activities.
- A setting that encourages innovation in programming and process improvement.
How You Will Make an Impact
- Deliver programming support for clinical studies and related regulatory outputs.
- Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
- Generate high-quality analysis outputs, including tables, figures, and listings.
- Write dataset specifications based on study protocols and statistical analysis plans.
- Build, refine, and support SAS macros and utility programs to streamline workflows.
- Solve complex technical issues and propose efficient programming solutions.
- Manage multiple project assignments while ensuring consistent quality and timely delivery.
- Collaborate effectively with statisticians, data managers, and other cross-functional partners.
Do you bring proven success in advanced statistical programming?
Required Skills & Experience
- 5-10 years of clinical or statistical programming experience.
- Advanced SAS programming skills with hands-on experience developing clinical datasets.
- Strong working knowledge of CDISC SDTM and ADaM standards.
- Experience in the pharmaceutical, biotech, or relevant industry.
- Ability to work independently and balance multiple concurrent assignments.
- Strong verbal and written communication abilities.
- Bachelor's degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field.
Preferred Qualifications
- Experience supporting regulatory submissions.
- Familiarity with additional programming tools (R, S-Plus, WinBUGS, Python, VBA, C++, etc.)
- Experience contributing to exploratory analyses or publications.
- Comfort working in a fast-paced, highly technical environment.
#dice
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.