IT Director, Development Business Partner
Kymera Therapeutics
August 26, 2026
On-site
Greater Boston
IT
How you’ll make an impact:
Kymera is seeking an IT Director, Development Business Partner (senior IT leader embedded within Development) to own technology strategy and execution across the Development portfolio.
Strategic Leadership
- Serve as the primary IT business partner across Development, building relationships with Clinical Operations, Clinical/Medical Development, Quality, Biometrics, Data Management, Regulatory, Program Management, Technical Operations, Medical Affairs, and Pharmacovigilance/Safety.
- Define and drive the technology roadmap balancing near-term delivery with Phase 3 scale and NDA readiness.
- Continuously improve and streamline Development processes and systems.
- Partner with the AI lead to identify, prioritize, and execute AI-enabled opportunities.
Technology Portfolio Ownership
- Lead implementations including Veeva Vault QMS, eTMF, and CTMS (validated, on time, high quality).
- Own strategy and vendor relationships for Regulatory, Quality, and Biometrics systems (fit-for-purpose, compliant, scalable).
- Partner with data analytics lead on integrations and analytic tools.
- Scope/evaluate new initiatives and maintain a 2–3 year application roadmap.
Execution and Delivery
- Lead requirements gathering, process mapping, and solution design in an environment without a dedicated PMO.
- Deliver validated, fit-for-purpose solutions meeting GxP and 21 CFR Part 11 (and other applicable standards).
- Drive change management, training, adoption, and ensure system integrations run smoothly.
Skills and experience you’ll bring
- 12+ years IT experience supporting Development in biotech/pharma.
- Experience taking a company through Phase 3, NDA submission, and commercialization.
- Hands-on Veeva Vault (QMS, eTMF, CTMS); strong clinical trial process and GxP/data standards knowledge.
- SAS-based (or equivalent) clinical submissions environment familiarity and validated systems governance.
- Regulatory Information Management systems experience.
- Practical interest in AI.
- Strong stakeholder management; vendor/partner management; ability to work 3–5 days on-site.
- Advanced life science/technical degree (plus).
Compensation
- Base salary range: $195,000–$275,000; eligibility for annual bonus, equity participation, and comprehensive benefits.
Kymera is seeking an IT Director, Development Business Partner (senior IT leader embedded within Development) to own technology strategy and execution across the Development portfolio.
Strategic Leadership
- Serve as the primary IT business partner across Development, building relationships with Clinical Operations, Clinical/Medical Development, Quality, Biometrics, Data Management, Regulatory, Program Management, Technical Operations, Medical Affairs, and Pharmacovigilance/Safety.
- Define and drive the technology roadmap balancing near-term delivery with Phase 3 scale and NDA readiness.
- Continuously improve and streamline Development processes and systems.
- Partner with the AI lead to identify, prioritize, and execute AI-enabled opportunities.
Technology Portfolio Ownership
- Lead implementations including Veeva Vault QMS, eTMF, and CTMS (validated, on time, high quality).
- Own strategy and vendor relationships for Regulatory, Quality, and Biometrics systems (fit-for-purpose, compliant, scalable).
- Partner with data analytics lead on integrations and analytic tools.
- Scope/evaluate new initiatives and maintain a 2–3 year application roadmap.
Execution and Delivery
- Lead requirements gathering, process mapping, and solution design in an environment without a dedicated PMO.
- Deliver validated, fit-for-purpose solutions meeting GxP and 21 CFR Part 11 (and other applicable standards).
- Drive change management, training, adoption, and ensure system integrations run smoothly.
Skills and experience you’ll bring
- 12+ years IT experience supporting Development in biotech/pharma.
- Experience taking a company through Phase 3, NDA submission, and commercialization.
- Hands-on Veeva Vault (QMS, eTMF, CTMS); strong clinical trial process and GxP/data standards knowledge.
- SAS-based (or equivalent) clinical submissions environment familiarity and validated systems governance.
- Regulatory Information Management systems experience.
- Practical interest in AI.
- Strong stakeholder management; vendor/partner management; ability to work 3–5 days on-site.
- Advanced life science/technical degree (plus).
Compensation
- Base salary range: $195,000–$275,000; eligibility for annual bonus, equity participation, and comprehensive benefits.