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Principal Biostatistician
Отличная позиция в стабильной клинической компании с прозрачным диапазоном зарплаты и сильным социальным пакетом. Работа над социально значимыми проектами (лечение редких заболеваний) и возможность удаленной работы делают вакансию крайне привлекательной.
Сложность вакансии
Роль требует ученой степени (Ph.D.), более 6 лет узкоспециализированного опыта в биотехе и глубоких знаний регуляторных стандартов (CDISC, SDTM, ADaM). Высокая ответственность за стратегию клинических испытаний и управление внешними вендорами повышает порог входа.
Анализ зарплаты
Предлагаемый диапазон $190,000–$231,000 полностью соответствует и даже немного превышает рыночные медианы для позиции Principal Biostatistician в Бостоне, который является одним из самых дорогих хабов в сфере Life Sciences.
Сопроводительное письмо
I am writing to express my strong interest in the Principal Biostatistician position at Entrada Therapeutics. With over six years of experience in the biotechnology industry and a Ph.D. in Statistics, I have developed a deep expertise in clinical trial design and the oversight of complex statistical deliverables. My background in managing CROs and ensuring the integrity of SDTM and ADaM datasets aligns perfectly with Entrada’s commitment to rigorous analytics and high-quality clinical development.
I am particularly drawn to Entrada’s innovative approach to intracellular targets and your robust portfolio in neuromuscular and retinal diseases. Having worked extensively with R and SAS to support clinical programs, I am eager to bring my experience in proposing novel statistical methodologies to accelerate your DMD and DM1 programs. I thrive in collaborative, fast-paced environments and look forward to the opportunity to contribute to your mission-driven team in Boston.
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Откликнитесь в entradatherapeutics уже сейчас
Присоединяйтесь к Entrada Therapeutics, чтобы внедрять инновационные статистические методы в разработку генетических лекарств и менять жизни пациентов.
Описание вакансии
The Organization
What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).
2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).
We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.
The Perfect Addition to Our Team
You are passionate about clinical trial research and driven to advance drug development through rigorous analytics. With a strong foundation in statistics and clinical methodologies, you combine classical techniques with cutting-edge innovations. You thrive in fast-paced settings, handle competing priorities with ease, and eagerly step in where needed. You are results-oriented and collaborative, and you thrive when build strong relationships across teams to deliver impactful solutions.
The Opportunity
Reporting to the Senior Director, 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.
- Previous vendor management experience is preferred.
- Previous experience in Neuromuscular, Ophthalmology or related TA is preferred.
- Excellent verbal and written communication skills with a strong attention for detail.
- 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 $190,000-$231,000. 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.#LI-JF1 #LI-Remote
Equal Opportunity Employer
Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.
Third Party Staffing Agencies
Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.
Privacy Statement
Entrada Therapeutics, Inc. (the “Entrada,” “we,” “us,” or “our”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement hereto understand how and when your data is being used.
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Навыки
- Statistics
- R
- SAS
- Python
- CDISC
- SDTM
- ADaM
- Clinical Trials
- Machine Learning
- Artificial Intelligence
Возможные вопросы на собеседовании
Проверка опыта работы с отраслевыми стандартами данных, необходимыми для подачи в регуляторные органы.
Опишите ваш опыт работы со стандартами CDISC, в частности с созданием спецификаций SDTM и ADaM. С какими сложностями вы сталкивались?
Вакансия предполагает использование инновационных подходов для ускорения программ.
Можете ли вы привести пример, когда вы предложили и внедрили инновационный статистический метод или дизайн исследования, который оптимизировал клиническую программу?
Роль включает контроль работы внешних организаций (CRO).
Как вы подходите к управлению качеством и соблюдению сроков при работе с внешними статистическими вендорами?
Оценка технических навыков и готовности использовать современные инструменты.
Каков ваш опыт использования языков программирования R и Python в дополнение к традиционному SAS для анализа клинических данных?
Проверка знаний в специфических терапевтических областях компании.
Есть ли у вас опыт работы в области нервно-мышечных заболеваний или офтальмологии, и как эта экспертиза помогает вам в разработке планов статистического анализа (SAP)?
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