Advanced sas programming skills with cdisc standards
Experience managing cros and external vendors
The role involves leading programming activities for clinical trials while ensuring timely and high-quality deliverables for regulatory submissions
Job Summary
The role involves leading programming activities for clinical trials while ensuring timely and high-quality deliverables for regulatory submissions.
Candidates will mentor programmers and foster a collaborative team environment committed to the company's C.O.R.E. values of Caring, Original, Resilient, and Egoless.
The position offers competitive compensation including base salary, performance bonus, equity grants, and comprehensive health and retirement benefits.
Matching Summary
The role involves leading programming activities for clinical trials while ensuring timely and high-quality deliverables for regulatory submissions.
Salary
Base: $270,000 - $295,000; Bonus/Equity: Performance bonus and equity grant opportunities; Benefits: Health, welfare, retirement, three weeks PTO, two shutdowns, paid sick leave
Skills & Requirements
Must-have
12-15 years clinical trial programming experience
Advanced SAS programming skills with CDISC standards
Experience managing CROs and external vendors
Support regulatory submissions (NDA/BLA/MAA)
Mentor team members in a fast-paced environment
Nice-to-have
Knowledge of AI use in drug development workflows
Experience with R or other statistical languages
Familiarity with cloud environments and scalable analytics
Alignment with C.O.R.E. values culture
Remote work experience in virtual teams
Key Requirements
Master's Degree in Statistics, Biostatistics, Mathematics, or Computer Science
Minimum 12-15 years progressive clinical trial programming experience
In-depth knowledge of CDISC standards (SDTM, ADaM) and controlled terminology
Experience supporting NDA, BLA, or MAA regulatory submissions
Strong leadership ability in small to mid-size biotech settings