Principal Scientist Oligonucleotide Chemistry

EMD Serono Research & Development Institute•Billerica, MA

11d•Onsite

About The Position

The Principal Scientist Oligonucleotide Chemistry is an onsite position in Billerica, MA. There will be approximately 10% domestic and international travel to meet business needs. Your Role: Plan and execute solid-phase oligonucleotide synthesis for SAR campaigns on several projects. Demonstrates understanding of the chemistry of nucleosides, nucleotides, and oligonucleotides as applied to siRNA, ASO and other oligonucleotide modalities. Design and implement scientific and synthesis strategies relating to the research and development of antisense and other synthetic oligonucleotide therapeutics. Strong laboratory skills in synthesis, purification, and characterization of complex siRNAs/ASO’s, expertise in state-of-the-art analytical techniques such as LC, MS, NMR. Demonstrate working knowledge of conjugation chemistry and techniques aimed at producing novel small molecule, peptides and antibody conjugates. Ability to analyze, interpret, and present data are a prerequisite current with scientific literature and understanding of the state of the art in oligonucleotide chemistry, purification, and screening strategies. Work with both internal chemistry team and external CRO’s to generate innovative solutions to synthetic and drug design challenges within the context of oligonucleotide drug discovery projects. Track progress against project timelines, generate regular status updates, and communicate progress and issues to management. Who You Are Minimum Qualifications: PhD in Oligonucleotide Chemistry and relevant experience in a drug discovery environment with 7+ years of oligonucleotide synthesis experience in industry. Master of Science in Chemistry/Medicinal Chemistry with 10+ years of experience in oligonucleotide synthesis experience in industry.

Requirements

PhD in Oligonucleotide Chemistry and relevant experience in a drug discovery environment with 7+ years of oligonucleotide synthesis experience in industry.
Master of Science in Chemistry/Medicinal Chemistry with 10+ years of experience in oligonucleotide synthesis experience in industry.

Nice To Haves

Excellent project/time management and problem-solving skills.
Excellent written and verbal communication skills, including making effective and compelling presentations in both large and small groups and communicating complex scientific and nonscientific issues to program teams.
Strong people skills and the ability to thrive in a team and goal driven environment.
Experience designing, synthesizing and purifying oligonucleotides to support research and scale up studies.
Proven track record of scientific contributions in oligonucleotide and conjugates research as evidenced by publications/presentations/patent applications and/or the identification of preclinical development candidates.

Responsibilities

Plan and execute solid-phase oligonucleotide synthesis for SAR campaigns on several projects.
Demonstrates understanding of the chemistry of nucleosides, nucleotides, and oligonucleotides as applied to siRNA, ASO and other oligonucleotide modalities.
Design and implement scientific and synthesis strategies relating to the research and development of antisense and other synthetic oligonucleotide therapeutics.
Strong laboratory skills in synthesis, purification, and characterization of complex siRNAs/ASO’s, expertise in state-of-the-art analytical techniques such as LC, MS, NMR.
Demonstrate working knowledge of conjugation chemistry and techniques aimed at producing novel small molecule, peptides and antibody conjugates.
Ability to analyze, interpret, and present data are a prerequisite current with scientific literature and understanding of the state of the art in oligonucleotide chemistry, purification, and screening strategies.
Work with both internal chemistry team and external CRO’s to generate innovative solutions to synthetic and drug design challenges within the context of oligonucleotide drug discovery projects.
Track progress against project timelines, generate regular status updates, and communicate progress and issues to management.