Director, Statistical Programming – Compound Level

Kymera Therapeutics, Inc.; Boston (MA); On-site; USD 160,000 - 275,000; Full time

Benefits offered by this job

Competitive compensation

Bonus eligibility

Equity participation

Comprehensive benefits

Job summary

Kymera Therapeutics, Inc. in Boston seeks an experienced Associate Director or Director of Statistical Programming to lead programming for a compound-level program across multiple clinical studies.

This role emphasizes strategic leadership, hands-on programming, and collaboration with cross‑functional teams to ensure high-quality, timely deliverables. The ideal candidate brings 8+ years in pharmaceutical/biotech statistics programming, deep CDISC SDTM/ADaM and Define-XML expertise, and strong

Qualifications

• 8+ years of statistical programming experience in pharma/biotech.
• Leadership of programming activities for a compound-level program.
• Oversight of CROs and external vendors with accountability for quality.

Responsibilities

• Lead statistical programming for a compound-level program with strategy, timelines and resource planning.
• Partner with Biostatistics, Clinical Development, Data Management and other teams to align timelines and quality.
• Manage in‑house programming projects and oversee in‑house programmers.
• Write SDTM/ADaM specs and develop datasets and TLFs for CSRs, publications and data requests.
• Support regulatory submissions (e.g., eCTD) and provide audits/inspection documentation.

Skills

SAS programming

CDISC SDTM/ADaM

Define-XML

Regulatory submissions

Leadership

Cross-functional collaboration

Education

MS in Statistics/Biostatistics/related field

Tools

R

Python

SAS

Job description

Kymera Therapeutics, Inc. in Boston seeks an experienced Associate Director or Director of Statistical Programming to lead programming for a compound-level program across multiple clinical studies.

This role emphasizes strategic leadership, hands-on programming, and collaboration with cross‑functional teams to ensure high-quality, timely deliverables. The ideal candidate brings 8+ years in pharmaceutical/biotech statistics programming, deep CDISC SDTM/ADaM and Define-XML expertise, and strong