ADME Project Lead, Genetic Medicines

100 Eli Lilly and Company; Boston (MA); On-site; USD 194,000 - 339,000; Full time

Benefits offered by this job

401(k)

Pension

Vacation benefits

Health benefits

Job summary

Lilly in Boston is seeking a skilled ADME/DMPK scientist to lead and innovate in a multidisciplinary team, supporting preclinical and clinical development of the genetic medicines portfolio.

You will integrate ADME/PK/PD endpoints with discovery data to guide design and delivery strategies, design hypothesis-driven studies, and mentor colleagues while contributing to regulatory communications and interactions with global authorities.

Qualifications

• Ph.D. in Biochemistry/Biology/Pharmacokinetics/Bioengineering/Pharmacology or related field.
• Greater than five years of ADME or PK/PD experience in pharma/biotech.

Responsibilities

• Lead ADME studies to support preclinical and clinical development of Lilly's genetic medicines portfolio.
• Integrate ADME, PK and PK/PD endpoints with discovery data to guide drug design and delivery strategies.
• Design, implement and interpret hypothesis-driven studies to address ADME, PK/PD and TK questions.
• Collaborate with cross-functional teams and mentor colleagues at all levels.
• Lead preparation of ADME portions of regulatory communications and interact with global authorities.

Skills

ADME expertise

PK/PD knowledge

Data analysis

Regulatory knowledge

Education

Ph.D. in Biochemistry/Biology/Pharmacokinetics/Bioengineering/Pharmacology

Tools

LC-MS

PCR

Immunoassay

Job description

Lilly in Boston is seeking a skilled ADME/DMPK scientist to lead and innovate in a multidisciplinary team, supporting preclinical and clinical development of the genetic medicines portfolio.

You will integrate ADME/PK/PD endpoints with discovery data to guide design and delivery strategies, design hypothesis-driven studies, and mentor colleagues while contributing to regulatory communications and interactions with global authorities.