Entrada Therapeutics

Principal Biostatistician

Entrada Therapeutics$203K — $247K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Statistics or related field with 6+ years of experience in biotech/pharmaceutical statistical analysis.
  • Broad experience with various statistical methods and familiarity with machine learning and AI.
  • Solid understanding of regulatory guidelines for drug development and submissions.
  • Strong statistical programming skills in R, SAS, and Python.
  • Familiarity with CDISC standards, including SDTM and ADaM specifications.
  • Proven vendor management experience.
  • Prior experience in Neuromuscular, Ophthalmology, or related therapeutic areas is preferred.

Responsibilities

  • Support statistical strategy and input on clinical development plans and study protocols.
  • Oversee biostatistics deliverables produced by external teams.
  • Provide strategic statistical input for protocols, reports, and presentations.
  • Review randomization procedures and manage randomization list production.
  • Ensure adherence to statistical requirements in study documentation.
  • Oversee outsourced CRO activities for quality and timeliness.
  • Create innovative statistical analysis tools through literature research.

Benefits

  • Comprehensive health, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) match offered.
  • Paid, gender-inclusive parental leave.
  • Education reimbursement available.
  • Holistic health and well-being support.
  • Discretionary time off and commuting benefits.
Full Job Description
The Opportunity

Reporting to the Head of Biometrics, this individual will contribute to daily statistical activities and support the development of statistical approaches for clinical trials. Working closely with internal and external stakeholders, you will help manage a growing portfolio of trials. This role also offers the opportunity to support the continued growth of the biostatistics function at Entrada and gain valuable experience in a collaborative, fast-paced environment.
Responsibilities
  • Support statistical strategy for assigned drug programs, including input to clinical development plans, clinical study concepts and protocols design, SAPs, clinical study reports, regulatory documentation and associated publications.
  • Accountable for oversight of the production of biostatistics deliverables (TFLs, including planned, post-hoc, and/or exploratory analyses) as performed by external resources.
  • Provide statistical strategy support and input in protocols, CSRs, and scientific presentations and manuscripts.
  • Review the randomization procedures and oversight of the production of randomization lists.
  • Review study Case Report Forms, data management plan and other data management related documentation to ensure that specific statistical requirements defined in the study protocol are met.
  • Oversee outsourced statistical CRO activities and deliverables, ensuring high quality and timely delivery.
  • Produce innovative tools and methodologies for statistical analysis through literature review.
  • Participate in the development of department strategies and cross functional initiatives on standards, infrastructure, and processes.
The Necessities

At Entrada, our passion for science, our devotion to patients and our values drives our behavior:
  • Humanity - We genuinely care about patients and about one another.
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.
  • Curiosity - We have a growth mindset and push conventional thought and theory.

To thrive on our team, you will need to come with:
  • Ph.D. in Statistics or a related field, with 6 + years of experience in statistical analysis within the biotech/pharmaceutical industry.
  • Experience with a broad array of statistical approaches and experience in proposing novel approaches to support acceleration of clinical programs. Knowledge in the latest developments in the analytical world including machine learning and artificial intelligence is a plus.
  • Solid understanding of regulatory guidelines on drug development, regulatory submissions, and statistical practice.
  • Strong statistical programming skills (R, SAS, Python).
  • Understanding of regulatory guidelines related to submission of datasets using CDISC, development of SDTM and ADaM specifications.
  • Strong vendor management experience.
  • Previous experience in Neuromuscular, Ophthalmology or related TA is preferred.
  • Excellent verbal and written communication skills, coupled with strong attention to detail and proactive mindset.
  • This is a US based remote position, with preference given to local New England based candidates. This role will require a minimum quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA. #LI-JF1 #LI-Remote
What We Offer: Meaningful Work, Fair Rewards, and Real Support

At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.

But we also know it is more than just pay. When you join Entrada, you'll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions - offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston's Seaport District, this puts you steps away from some of the best the city has to offer.

"Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward - and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward."

- Kerry Robert, SVP of People

The salary for this opportunity ranges from $203,000-$247,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate's skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range.

About Entrada Therapeutics

Entrada Therapeutics is a biotechnology company that is focused on developing therapies for diseases that are difficult to treat. The company's proprietary platform technology allows for the delivery of large molecules, such as proteins and nucleic acids, into cells and tissues that were previously inaccessible. This technology has the potential to transform the treatment of a wide range of diseases, including genetic disorders, cancer, and autoimmune diseases. Entrada Therapeutics was founded in 2016 and is headquartered in Waltham, Massachusetts.
Learn more about Entrada Therapeutics
Size
50 employees
Market Cap
$485.5 million
Industry
Founded
2016
NASDAQ

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