Stop applying to remote jobs that are already dead.
Every listing checked, aged honestly, expired when filled.

All listings

Senior Principal Statistical Programmer

United States lead
still open verified 2h ago posted 3d ago seen 2h ago
Apply at jobs.ashbyhq.com

This is the employer's own posting, not a copy on a job board.

What we know

Is it still open?

Confirmed still open

Last checked 2h ago — checked against the employer's own applicant tracking system, which is the company answering directly.

We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.

Check this listing's status as JSON

How old is it?

Posted 3d ago

The date the source published, not the day we noticed it (2026-09-28). Last seen at its source 2h ago.

We have tracked this listing since 29 Sep 2026 (3 days). The employer's own board has carried it every time we have read it, most recently 2 hours ago.

Is it remote?

Remote - US

That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.

Who may apply?

United States

The description states no restriction of its own. This is the source's own tag.

Pay not stated

Similar roles pay $182.5k–250k/yr

Middle 50% of 841 listings that do state pay — Engineering · Lead · United States · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.

Skills named in the ad

Code ReviewMachine LearningPartnershipsPythonStatistics

Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.

Carried by 1 source

The listing

JOB SUMMARY

We are seeking a Senior Principal Statistical Programmer to join our Clinical Development team at Iambic. This role will be a key contributor in supporting statistical programming activities for clinical trials, from Phase I through regulatory submission. The ideal candidate is a hands-on leader with deep technical expertise in SAS programming and CDISC standards, as well as a strong understanding of regulatory requirements and clinical trial processes. Additionally, this role will interface with the data science and machine learning groups and provide collaboration efforts to bridge clinical and existing AI infrastructure.

KEY RESPONSIBILITIES

  • Lead the design, development, validation, and maintenance of SAS programs for the generation of SDTM, ADaM, and TLFs (tables, listings, and figures).

  • Ensure compliance with CDISC standards (SDTM and ADaM), FDA/EMA regulatory guidelines, and internal SOPs.

  • Collaborate closely with Biostatisticians, Data Managers, and Clinical Operations teams to define programming requirements and timelines.

  • Perform quality control and peer review of deliverables to ensure accuracy, consistency, and adherence to specifications.

  • Act as the technical subject matter expert on statistical programming and mentor junior programmers.

  • Support the preparation of clinical study reports (CSRs), regulatory submission packages (e.g., eCTD, ISS/ISE), and responses to regulatory agencies.

  • Participate in the development and refinement of departmental processes, templates, and tools to optimize efficiency and quality.

  • Contribute to vendor oversight and provide technical leadership when outsourcing programming activities.

QUALIFICATIONS

  • Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Life Sciences, or a related field.

  • Minimum of 10 years of experience in statistical programming in the pharmaceutical, biotechnology, or CRO industry. Oncology experience preferred.

  • Proficiency in SAS/Base, SAS/Macro, SAS/SQL, and SAS/Graph. Familiarity with python preferred.

  • Strong experience with CDISC standards (SDTM and ADaM) and familiarity with define.xml and Pinnacle 21.

  • Experience supporting regulatory submissions to FDA and/or EMA.

  • Excellent problem-solving skills, attention to detail, and the ability to work both independently and as part of a cross-functional team.

  • Exposure to cloud-based data systems or programming in a validated GxP environment preferred.

ABOUT IAMBIC THERAPEUTICS

Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai.

MISSION & CORE VALUES

Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies.

PAY AND BENEFITS

We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play.

Apply at jobs.ashbyhq.com