WAVE Life Sciences Ltd.

Associate Director, Translational Toxicology, Preclinical Development

WAVE Life Sciences Ltd.$170K — $230K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • DVM/PhD or PhD in biology, toxicology or related field; Board certification in toxicology preferred.
  • 7+ years of relevant experience in preclinical safety assessment of novel therapeutic entities.
  • Experience with regulatory submissions and responses required.
  • In-depth knowledge of safety pharmacology and investigative toxicology.
  • Familiarity with nonclinical regulatory documents and interactions with regulatory authorities.

Responsibilities

  • Represent the Preclinical and Clinical Development Sciences (PCDS) team on Program Teams.
  • Coordinate and liaise between PCDS and other departments such as Regulatory Affairs and Clinical Operations.
  • Provide risk assessment and develop de-risking strategies for discovery programs.
  • Design preclinical strategies for Discovery and Development candidates.
  • Lead the design and coordination of toxicity studies, ensuring integration with bioanalytical data.
  • Collaborate with other teams to interpret animal models for efficacy and toxicity assessment.
  • Drive early investigations into mechanisms of toxicity to manage safety liabilities proactively.
  • Offer strategic guidance to project teams regarding toxicology results and their implications.

Benefits

  • Comprehensive medical, dental, and vision insurance plans.
  • Generous paid time off including company-wide shutdowns.
  • 401K with matching contributions.
  • Employee Stock Purchase Program for long-term investment opportunities.
  • Disability and life insurance coverage.
Full Job Description
Description:

Wave Life Sciences is seeking a highly motivated individual to join the Preclinical and Clinical Development Sciences team in Lexington, Massachusetts. The candidate will be expected to provide scientific expertise and leadership across the Discovery and Development portfolio by contributing to the safety assessment of novel therapeutic oligonucleotides intended for the treatment of rare diseases. The candidate should possess an in-depth understanding of safety pharmacology, investigative and regulatory toxicology, and have experience designing and critically evaluating results of exploratory and GLP-compliant toxicology studies. Previous experience in authoring and reviewing nonclinical regulatory documents as well as interactions with regulatory authorities is required as is a background in the safety assessment of drugs intended to treat diseases of the hepatic, kidney, muscular and central nervous systems.

Experience:
  • DVM/PhD or PhD in biology, toxicology or related field, Board certification in toxicology is highly desirable.
  • Relevant experience (7+ years) in preclinical safety assessment of novel therapeutic entities.
  • Experience with regulatory submissions and responses.

Responsibilities:
  • This position will be part of the Preclinical and Clinical Development Sciences (PCDS) team supporting development as a primary representative of PCDS on Program Teams.
  • Represent PCDS at team meetings and coordinate between PCDS and other functions including CMC, Regulatory Affairs, Clinical Operations, and Platform and Discovery Sciences.
  • Provide risk assessment and de-risking strategies for discovery programs.
  • Design preclinical strategies for Discovery and Development candidate molecules.
  • Design toxicity studies: coordinate with Preclinical Outsourcing for placement and monitoring of the studies as well as the Bioanalytical and DMPK groups regarding integration of bioanalysis and toxicokinetic aspects into these studies to ensure on-time delivery of key data and study reports.
  • Work with Platform Discovery Sciences, Translational Medicine and program teams to utilize and interpret animal models of diseases for efficacy/tolerability assessment and PK/PD evaluation.
  • Lead the development of early hypothesis-driven investigation into mechanisms of toxicity for the proactive management of potential safety liabilities and communication of impact to teams.
  • Provide strategic guidance to project teams and senior management including evaluation of conclusions and potential impact of toxicology results on program and clinical/regulatory strategy.
  • Lead issue-resolution teams, driving the science for investigative and discovery toxicology as needed.
  • Provide leadership as a key member of the Preclinical Development Leadership Team with opportunities for continual organizational advancement.

Key Skills:
  • Knowledge of GLP compliance and relevant ICH & FDA guidance documents.
  • Outstanding interpersonal skills and verbal and written communication skills.
  • Ability to work effectively both independently and collaboratively in a dynamic team-oriented environment.
  • Ability to oversee CRO interface, as appropriate, to deliver high quality, cost-effective, and timely safety assessment.
  • Ability to collaborate with colleagues, internally and externally, to execute on the appropriate studies to support selection of therapeutic targets, and the identification and development of new drug candidates.
  • Ability to travel to monitor out-sourced studies.
  • Outstanding organizational skills/ability to prioritize and deliver in timely fashion.

Pay Range External Disclosure Statement

The annual base salary range for this position is $170,000 - 230,000.

The range provided is based on what we believe is a reasonable estimate for the annual base salary pay range for this position at the time of posting. Actual annual base salary will vary based on several factors including, but not limited to, relevant skills, experience, qualifications, position criticality, and internal equity. This position is eligible for a discretionary annual bonus and discretionary stock-based long-term incentives. In addition to compensation, Wave offers a comprehensive and competitive range of benefits designed to support our employees' and their families physical and financial health and overall well-being. These include, but are not limited to, company-sponsored medical, dental, vision, life, long and short-term disability insurances, generous paid time off (including a week-long company shutdown in the Summer and the Winter), 401K participation with matching contributions, and Employee Stock Purchase Program.

About WAVE Life Sciences Ltd.

WAVE Life Sciences Ltd. is a biotechnology company that specializes in the development of nucleic acid therapeutics. The company's proprietary platform allows for the design and optimization of synthetic nucleic acid molecules that can selectively target and modulate the expression of disease-causing genes. WAVE's pipeline includes programs in Huntington's disease, Duchenne muscular dystrophy, and various other genetic disorders. The company was founded in 2012 and is headquartered in Singapore, with additional offices in Cambridge, Massachusetts and Tokyo, Japan.
Learn more about WAVE Life Sciences Ltd.
Size
235 employees
Market Cap
$522.8 million
Industry
Net Income
-$149.9 million
Founded
2012
5 Year Trend
+106.5%
Revenue
$20 million
NASDAQ

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