Senior In Vivo Pharmacology Scientist - Gene Therapy

Integrated Resources, Inc.; Boston (MA); Sur place; USD 130 000 - 170 000; Plein temps

Résumé du poste

Integrated Resources, Inc. is seeking an in vivo pharmacology Senior Scientist to contribute to a Gene Therapy research program in Boston.

The role involves executing experiments in rodent models to support discovery and optimization of novel genetic medicines, with emphasis on data integrity and cross-team collaboration. Responsibilities include designing studies, developing models, and communicating results in study reports while maintaining Lilly-compliant documentation.

Qualifications

• Bachelor's or Master’s degree in life sciences or related field with 3–5 years industry/ CRO experience.
• Hands-on experience with rodent handling, dosing, and blood collection in mice and rats.
• Strong data analysis and ability to interpret experiments independently.

Responsabilités

• Design and execute in vivo pharmacology experiments to characterize activity, distribution, and clearance of genetic medicines in rodent models.
• Assist in development and characterization of novel in vivo models.
• Collaborate with Preclinical, toxicology, and PK/PD teams to translate discovery to development.
• Prepare written and verbal communications for study reports and team meetings.
• Maintain accurate electronic notebooks following Lilly-style quality standards and Good Documentation Practices.
• Ensure compliance with health and safety regulations.

Connaissances

Rodent handling

In vivo pharmacology

Data analysis

Scientific communication

Formation

BS/MS in life sciences

Description du poste

Integrated Resources, Inc. is seeking an in vivo pharmacology Senior Scientist to contribute to a Gene Therapy research program in Boston.

The role involves executing experiments in rodent models to support discovery and optimization of novel genetic medicines, with emphasis on data integrity and cross-team collaboration. Responsibilities include designing studies, developing models, and communicating results in study reports while maintaining Lilly-compliant documentation.