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The QA Specialist II/III leads investigations of customer complaints and critical deviations, ensuring compliance with quality standards and mentoring team members.

The Senior Safety Scientist supports drug safety and pharmacovigilance, overseeing safety profiles, risk management, and study management, while collaborating within global teams.

The Senior Patent Counsel will manage intellectual property assets, create IP strategies, conduct patent analyses, and offer legal advice in a biotech context.

As Global Development Leader for CVRM, you will oversee late-stage clinical development strategies and lead cross-functional teams to ensure effective execution of clinical programs and regulatory submissions.

The Sr. Independent Medical Education Manager influences funding for medical education, guiding the business to close health gaps while managing IME budgets and assessing educational needs.

Collaborate with partners to measure skills training effects, implement data quality procedures, apply statistical methods, and present findings.

Assist in building a database for small molecule attributes, conducting data analysis, and supporting early-stage risk assessments in pharmaceutical development.

Assist in designing data analytics tools, maintain analytic products, perform data cleaning, and support process improvement within the Learning & Skill Development team.

The intern will assist in method development for LC-MS assays, focusing on drug candidate analysis in biological matrices. Responsibilities include sample processing, data analysis, and presenting results.

Interns will engage in research involving machine learning applied to molecular sciences, contribute to publications, and develop code for research methods.