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parabilismed
Страна
США
Зарплата
265 000 $ – 305 000 $
+500% приглашений

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DirectorУдалённоПолная занятость

Senior Director, Clinical Sciences

Оценка ИИ

Исключительная вакансия в стабильной компании с недавним крупным финансированием ($305 млн). Предлагает высокую зарплату, работу над прорывными технологиями и четкие ценности, ориентированные на пациента.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Высокая сложность обусловлена требованием более 10 лет опыта в биотехе, глубокой научной экспертизы (PhD/PharmD) и обязательного владения инструментами ИИ. Роль подразумевает лидерство в разработке стратегий для инновационных и сложных терапевтических платформ.

Анализ зарплаты

Медиана285 000 $
Рынок250 000 $ – 320 000 $
Оценка ИИ

Предлагаемый диапазон $265k–$305k полностью соответствует рыночным стандартам для позиции Senior Director в Кембридже, штат Массачусетс, который является одним из самых дорогих и конкурентных биотех-хабов в мире. Указанная зарплата находится на уровне медианы или чуть выше для опытных специалистов в этой области.

Сопроводительное письмо

I am writing to express my strong interest in the Senior Director, Clinical Sciences position at Parabilis Medicines. With over a decade of experience in clinical development and a deep background in oncology and complex therapeutic areas, I am inspired by Parabilis’ success in drugging the 'undruggable' with the Helicon™ platform. My expertise in Phase 1-3 trial design and my track record of successful regulatory interactions align perfectly with your mission to advance zolucatetide and your expanding pipeline.

Throughout my career, I have prioritized the integration of translational insights into clinical strategy to drive efficient decision-making. I am particularly impressed by Parabilis’ commitment to leveraging AI-enabled tools, a practice I have actively integrated into my own workflow to enhance data interpretation and operational efficiency. I am eager to bring my strategic leadership and scientific rigor to your team in Cambridge to help transform treatment possibilities for patients with urgent unmet needs.

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Откликнитесь в parabilismed уже сейчас

Присоединяйтесь к лидерам в разработке инновационных пептидных препаратов и возглавьте клиническую стратегию будущего!

Описание вакансии

Why Join Us?

As a member of the Parabilis Medicines team, you will be a part of an organization dedicated to creating extraordinary medicines for diseases with urgent unmet needs, harnessing our proprietary peptide platform to transform treatment possibilities for patients. Parabilis is a clinical-stage biopharmaceutical company dedicated to unlocking high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that are inaccessible to traditional drug modalities.

Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its lead asset, zolucatetide (FOG-001), is a first-in-class, clinically validated direct inhibitor of the interaction between β-catenin and the T-cell factor (TCF) family of transcription factors, implicated in millions of cancer cases annually, including in colorectal cancer, desmoid tumors, hepatocellular carcinoma and a range of other Wnt/β-catenin-driven tumors. In Phase 1 clinical trials, zolucatetide produced the first-ever clinical evidence that it can directly inhibit this interaction, once previously considered “undruggable” despite its role across multiple cancer types. Parabilis is also advancing investigational degraders of ERG and ARON into clinical development for the treatment of prostate cancer, as well as progressing other preclinical programs. Backed by a recent $305 million Series F financing, Parabilis is entering an exciting phase of growth and execution.

What’s the opportunity?

Parabilis Medicines is seeking a Senior Director, Clinical Sciences to provide scientific and strategic leadership across our clinical development programs. This role is central to translating discovery and preclinical innovation into high-quality, data-driven clinical development strategies that advance our pipeline efficiently and responsibly.

As Senior Director, Clinical Sciences, you will shape clinical science strategy from early clinical planning through execution, ensuring scientific rigor, regulatory alignment, and cross-functional integration. You will be a key scientific voice in clinical trial design, interpretation of clinical data, and external engagement, with a direct impact on the success of Parabilis’ clinical programs and long-term company goals.

As part of this role you will:

  • Lead and own clinical science strategy for one or more clinical programs across development stages
  • Drive scientific input into protocol design, endpoint selection, and clinical development plans
  • Serve as a core contributor to regulatory interactions, governance decisions, and program reviews
  • Influence portfolio strategy through integrated clinical and translational insights
  • Partner closely with Clinical Operations to ensure scientifically sound and feasible trial execution
  • Interpret and contextualize clinical, biomarker, and safety data to inform decision-making
  • Contribute to regulatory documents (INDs, IBs, briefing packages) and regulatory interactions
  • Support investigator meetings, advisory boards, and external scientific communications
  • Ensure consistency of scientific messaging across internal and external stakeholders
  • Mentor and guide junior clinical scientists as the organization grows
  • Leverage AI-enabled tools to enhance clinical insights, literature analysis, data interpretation, and operational efficiency

What you’ll need to be successful:

  • PhD, PharmD, or equivalent advanced degree in life sciences, medicine, or a related field
  • 10+ years of experience in clinical development or clinical sciences within biotech or pharmaceutical settings
  • Direct experience supporting or leading clinical trials (Phase 1–3 preferred)
  • Proven track record of contributing to successful clinical programs and regulatory milestones
  • Deep understanding of clinical trial design, endpoints, and regulatory requirements
  • Experience working with clinical data systems, trial databases, and scientific literature platforms
  • Familiarity with biomarker and translational data integration
  • Strong scientific writing and data presentation skills
  • Experience in rare disease, oncology, immunology, or other complex therapeutic areas (as applicable to Parabilis’ pipeline)
  • Prior leadership or matrix-management experience
  • Experience interacting with regulatory agencies and external experts
  • Strong strategic thinking combined with hands-on execution
  • Comfort operating in a fast-paced, evolving biotech environment
  • Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.

Core Values

Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.

  • Growth-Minded. We’re inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.
  • In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.
  • Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.
  • All-In. We’re All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.

The base salary range for this position is [$265,000–$305,000 per year], depending on experience, qualifications, and internal practices. Parabilis’s total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitivebenefits designed to support our employees’ overall well-being.

As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

30 Acorn Park Drive    |     Cambridge, MA 02140    |    www.parabilismed.com

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Создайте идеальное резюме с помощью ИИ-агента

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Навыки

  • Clinical Development
  • Clinical Trials
  • Oncology
  • Regulatory Affairs
  • Scientific Writing
  • Biomarkers
  • Translational Medicine
  • Artificial Intelligence
  • Drug Discovery
  • Pharmacology

Возможные вопросы на собеседовании

Вакансия требует обязательного использования ИИ в текущей работе. Работодателю важно понять практическую ценность этого навыка.

Расскажите о наиболее инновационном способе использования инструментов ИИ в вашей практике для повышения эффективности клинических исследований или анализа данных.

Компания работает с уникальной платформой Helicon™. Кандидат должен понимать специфику работы с новыми модальностями.

С какими основными научными и регуляторными вызовами вы сталкивались при переводе доклинических инноваций в клиническую стадию для принципиально новых классов препаратов?

Роль предполагает руководство стратегией клинических программ.

Опишите ваш опыт разработки дизайна протокола для фазы 1/2, где выбор конечных точек имел решающее значение для успеха программы.

Позиция Senior Director требует навыков взаимодействия с государственными органами.

Можете ли вы привести пример успешного взаимодействия с FDA или EMA, которое существенно повлияло на план клинического развития вашего продукта?

Работа в биотехе требует умения работать в кросс-функциональных командах.

Как вы балансируете между научной строгостью дизайна исследования и операционной осуществимостью при работе с отделом Clinical Operations?

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parabilismed
Страна
США
Зарплата
265 000 $ – 305 000 $