Oligonucleotide Chemistry Lead for RNAi Scale-Up

BioSpace

Indianapolis (IN)

On-site

USD 126,000 - 205,000

Full time

5 days ago
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Benefits offered by this job

401(k) plan
Pension
Well-being benefits

Job summary

Lilly Genetic Medicines is seeking a collaborative scientist in Indianapolis to lead the discovery oligosynthesis scale‑up team and accelerate RNAi Therapeutics from pre‑clinical to clinical development.

You will mentor a multidisciplinary group, drive synthesis from 150umol to 6mmol scales, and partner with CMC/Development teams to deliver essential materials for key studies. Strong communication and leadership are required.

Qualifications

  • PhD with 2+ years oligonucleotide synthesis experience
  • MS with 5+ years oligonucleotide synthesis experience

Responsibilities

  • Lead the Lilly Genetic Medicines discovery oligosynthesis scale‑up team to accelerate RNAi therapeutics from pre‑clinical to clinical development
  • Utilize synthesis methodologies to support internal capabilities and team growth through coaching and leadership
  • Collaborate with RNAi discovery chemistry teams to validate synthesis requirements from 150umol to 6mmol scales
  • Communicate results to project leads and cross‑functional teams to ensure seamless scale‑up operations
  • Support lead drug candidate discovery and provide materials for key studies with CMC and Development teams
  • Demonstrate expertise in modern organic and nucleic acid chemistry and improve synthetic methods
  • Oversee and prioritize work of scale‑up team members to meet timelines
  • Encourage diverse perspectives and ownership of outcomes among team members

Skills

Team leadership
Troubleshooting
Chromatography
LC-MS
Interdisciplinary work
Communication

Education

PhD in relevant science
MS in relevant science

Tools

AKTA
Agilent LC-MS
UPLC

Job description

Lilly Genetic Medicines is seeking a collaborative scientist in Indianapolis to lead the discovery oligosynthesis scale‑up team and accelerate RNAi Therapeutics from pre‑clinical to clinical development.

You will mentor a multidisciplinary group, drive synthesis from 150umol to 6mmol scales, and partner with CMC/Development teams to deliver essential materials for key studies. Strong communication and leadership are required.

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