Full-Time
Clinical SAS Programmer
Katalyst Healthcares & Life Sciences
51-200 employees
Clinical trial management software and services
No salary listed
Newark, NJ, USA
In Person
 Biology & Biotech (2) |
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- MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
- Experience in providing statistical programming support to early and late phase clinical trials.
- Excellent skills in SAS programming and statistical reporting.
- Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
- Familiarity with FDA and ICH regulations and guidelines.
- Excellent problem-solving skills.
- Good written and verbal communication skills and organizational and documentation skills.
- Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
- Ability to prioritize and multi-task effectively.
- Demonstrated positive attitude and the ability to work well with others.
- Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
- Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
- Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
- Provides input in the design and development of case report forms and clinical databases.
- Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
- Programs for quality checks for clinical study raw data and report the findings to Data Management.
- Provides input in the design and development of case report forms and clinical study databases.
- Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.
Katalyst Healthcares & Life Sciences provides a Clinical Trial Management Solution called EasyCDM Suite that covers the full lifecycle of clinical trials. The product supports study design, data capture, medical coding, and data management to streamline processes for clients in pharmaceutical, biopharmaceutical, medical device, cosmeceuticals, and food and beverage industries. The system works by organizing trial data in a unified platform, enabling electronic data capture (EDC), coding, data validation, and workflow management, while consulting services assist with implementation and optimization. The company differentiates itself through a combined offering of software, consulting, and services that aim to accelerate drug development while maintaining quality and safety standards. The goal is to simplify business challenges, maximize human potential, and improve health outcomes worldwide through life science innovations.
Company Size
51-200
Company Stage
N/A
Total Funding
N/A
Headquarters
South Plainfield, New Jersey
Founded
2016
Simplify's Take
What believers are saying
- Hiring 735 positions signals strong contract staffing expansion.
- Global CRO services enhance competitive positioning worldwide.
- Active jobs in Burlington MA, Newark NJ, San Diego CA diversify geography.
What critics are saying
- Medidata Rave and Veeva Vault erode EasyCDM sales in 12-24 months.
- FDA 2025 AI mandate forces EasyCDM upgrades or client loss in 6-12 months.
- Oracle-Certara acquisition outcompetes consulting contracts in 18-24 months.
What makes Katalyst Healthcares & Life Sciences unique
- EasyCDM Suite streamlines clinical trials from study design to data management.
- Serves pharmaceutical, biopharma, medical devices, cosmeceuticals, and food sectors.
- Combines consulting services with EasyCDM for accelerated drug development.
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