Director, Toxicology Study Quality & GLP Compliance

Novartis AG; Cambridge (MA); Hybrid; USD 186,000 - 345,000; Full time

Benefits offered by this job

Health, life and disability benefits

401(k) with company match

Generous vacation and time-off

Job summary

Novartis AG in Cambridge, MA seeks a Director to lead the PCS Study Quality and Compliance team, driving long-term strategy and yearly goals. The role focuses on GLP-compliant toxicology studies, data management, and readiness of SEND datasets for regulatory submissions.

The position requires extensive toxicology experience, strong leadership, and fluency in English. It is a hybrid role with responsibilities spanning data systems, training, and cross-functional collaboration.

Qualifications

• PhD/advanced degree in biology-related sciences with extensive toxicology experience preferred.
• GLP guidelines knowledge and toxicology study oversight.
• Familiarity with SEND or related data requirements.

Responsibilities

• Lead and provide strategic oversight to the PCS Study Quality and Compliance team.
• Modernize group functionality with tracking, management, and data analytics software across toxicology.
• Oversee toxicology study data management and prepare data for internal data warehouse.

Skills

Leadership

Communication

Data Analysis

Problem Solving

Ethics

Mentorship

Education

Advanced degree in biology-related sciences

BS in biology-related sciences

25+ years of relevant industry experience

Tools

Smartsheet

Job description

Novartis AG in Cambridge, MA seeks a Director to lead the PCS Study Quality and Compliance team, driving long-term strategy and yearly goals. The role focuses on GLP-compliant toxicology studies, data management, and readiness of SEND datasets for regulatory submissions.

The position requires extensive toxicology experience, strong leadership, and fluency in English. It is a hybrid role with responsibilities spanning data systems, training, and cross-functional collaboration.