Senior Translational Pharmacology Scientist (Hybrid)

Elanco

Indianapolis (IN)

Hybrid

USD 120,000 - 180,000

Full time

5 days ago
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Benefits offered by this job

Hybrid work environment
Travel up to 30%

Job summary

Elanco, headquartered in Indianapolis, IN, is seeking a (Senior) Research Scientist in the Non-Clinical Development team to advance translational pharmacology. The role focuses on guiding early drug development by bridging in vitro findings with clinical efficacy and leading cross-functional translational efforts.

You will design translational studies, oversee CROs, and develop PK/PD biomarker strategies to support therapeutic dosing, while collaborating with Safety and DMPK teams and project

Qualifications

  • DVM or PhD required with relevant postdoctoral training or residency in pharma/biotech.
  • Experience in early drug development and translational pharmacology.
  • Demonstrated ability to lead cross-functional teams and manage CROs.

Responsibilities

  • Design and coordinate translational pharmacology studies for profiling compounds.
  • Analyze drug mechanisms, target biology, and disease pathophysiology to reduce development risk.
  • Provide technical oversight for in vivo studies and CRO partnerships.
  • Define and implement PK/PD biomarker strategies to support dosing decisions.
  • Lead translational analyses and communicate findings to stakeholders.

Skills

In Vivo pharmacology
Biomarker strategies
Translational pharmacology
CRO collaboration
Scientific leadership
English communication

Education

DVM (Doctor of Veterinary Medicine)
PhD in Veterinary Medicine or related field

Tools

PK/PD analysis
In Vivo assays

Job description

Elanco, headquartered in Indianapolis, IN, is seeking a (Senior) Research Scientist in the Non-Clinical Development team to advance translational pharmacology. The role focuses on guiding early drug development by bridging in vitro findings with clinical efficacy and leading cross-functional translational efforts.

You will design translational studies, oversee CROs, and develop PK/PD biomarker strategies to support therapeutic dosing, while collaborating with Safety and DMPK teams and project

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