Alnylam Pharmaceuticals

Vice President, Toxicology

Alnylam Pharmaceuticals$284K — $385K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Toxicology, Pathology, or related field.
  • 15+ years in pharmaceutical/biotech with a focus on regulatory toxicology.
  • Leadership experience managing scientific teams or departments.
  • Experience in preparing and supporting global regulatory submissions.
  • Ability to interpret complex datasets across multiple disciplines.
  • Creative problem-solving skills in predictive toxicology challenges.
  • Strong organizational and leadership skills in fast-paced environments.
  • Excellent interpersonal and collaboration skills across teams.
  • Effective written and verbal communication abilities.
  • Interest in therapeutic areas related to Alnylam's research.

Responsibilities

  • Lead a team of toxicologists and technical staff to enhance scientific excellence and collaboration.
  • Provide strategic direction for nonclinical safety assessments and regulatory submissions.
  • Collaborate across various scientific disciplines to ensure project integration.
  • Engage with regulatory authorities to support submissions and product defense.
  • Design nonclinical development programs for drug candidates and regulatory filings.
  • Manage nonclinical studies and programs both internally and via CRO partnerships.
  • Prepare and review scientific/regulatory documents for quality and clarity.
  • Partner with teams to design toxicology studies for development candidates and technologies.
  • Present findings and safety strategies to leadership and regulatory officials.
  • Mentor toxicologists and scientists to bolster organizational expertise.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • Lifestyle reimbursement program.
  • Flexible spending and health savings accounts.
  • 401(k) with a generous company match.
  • Paid time off, wellness days, and holidays.
  • Company-wide recharge breaks.
  • Generous family resources and leave programs.
Full Job Description
Overview:

The successful candidate will join an experienced team of toxicologists providing discovery and development support across a strong and diverse pipeline of programs spanning multiple disease areas. In addition to leading and contributing to regulatory toxicology activities, this role will place strong emphasis on supporting research initiatives and providing scientific leadership within the broader Early Development department.

Responsibilities:

  • Lead and oversee a team of toxicologists and technical staff, fostering scientific excellence, collaboration, and professional development.
  • Provide strategic leadership for nonclinical safety assessment programs supporting discovery, development, and regulatory submissions.
  • Collaborate effectively across disciplines, including pathology, DMPK, biology, clinical, regulatory, and pharmacology, ensuring strong cross-functional integration.
  • Engage effectively with regulatory authorities, supporting product defense and contributing to successful regulatory submissions and approvals.
  • Design and implement scientifically robust and strategically aligned nonclinical development programs to support advancement of drug candidates and regulatory filings.
  • Lead and manage nonclinical studies and programs across a portfolio of projects, conducted internally and through CRO partners, either directly or through direct reports.
  • Prepare and critically review scientific and regulatory documents to ensure high quality, clarity of presentation, and sound scientific interpretation.
  • Partner with cross-functional teams to design investigative toxicology studies supporting development candidates and platform technology evaluations.
  • Present key findings and safety strategies to program teams, R&D leadership, and regulatory authorities.
  • Mentor and develop toxicologists and scientists, helping build organizational expertise in pharmaceutical toxicology and nonclinical safety.


Qualifications:

  • PhD in Toxicology, Pathology, or a related scientific discipline.
  • 15+ years of experience in the pharmaceutical or biotechnology industry, with demonstrated expertise and accomplishments in regulatory toxicology.
  • Proven leadership experience managing departments, groups, or teams within a scientific organization.
  • Demonstrated experience preparing and supporting global regulatory submissions and associated documentation.
  • Strong ability to interpret and integrate complex datasets across multiple disciplines, including pharmacology, DMPK, toxicology, and pathology, with a focus on assessing clinical relevance and impact.
  • Proven ability to apply creative and strategic approaches to resolving challenges in predictive toxicology.
  • Strong problem-solving skills, with the ability to remain highly organized and lead effectively in a fast-paced environment with evolving priorities.
  • Excellent interpersonal skills and a demonstrated ability to collaborate across diverse cross-functional teams.
  • Excellent written and verbal communication skills.
  • Strong interest in the therapeutic and scientific areas aligned with Alnylam's research focus.

#LI-KB1 #LI-Onsite

U.S. Pay Range

$284,800.00 - $385,200.00

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).

Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.

Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers

About Alnylam Pharmaceuticals

Alnylam Pharmaceuticals is a biotechnology company that focuses on RNA interference (RNAi) therapeutics. The company's products are designed to silence specific genes that cause diseases. Alnylam's pipeline includes products for the treatment of genetic, cardio-metabolic, and hepatic infectious diseases. The company was founded in 2002 and is headquartered in Cambridge, Massachusetts.
Learn more about Alnylam Pharmaceuticals
Size
1,665 employees
Market Cap
$28.7 billion
Industry
Net Income
-$858.2 million
Founded
2002
5 Year Trend
+78.1%
Revenue
$492.8 million
NASDAQ

Similar Jobs

More Jobs at Alnylam Pharmaceuticals

More Pharmaceuticals & Biotech Jobs

Find similar Vice President, Toxicology jobs: