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Страна
США
Зарплата
211 000 $ – 264 000 $
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DirectorГибридПолная занятость

Director, Clinical Development

ИИОценка ИИ

Отличная позиция в инновационной компании с четкой миссией и конкурентной заработной платой. Высокий балл обусловлен прозрачностью условий, значимостью разрабатываемых продуктов и сильным социальным пакетом.


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Сложность вакансии

ЛегкоСложно
ИИОценка ИИ

Высокий уровень сложности обусловлен требованием ученой степени (PhD/PharmD), минимум 8 лет опыта в индустрии и глубокой экспертизы в онкологии. Роль подразумевает высокую ответственность за стратегическое планирование и руководство кросс-функциональными командами.

Анализ зарплаты

Медиана245 000 $
Рынок210 000 $ – 280 000 $
ИИОценка ИИ

Предложенная зарплата ($211k - $264k) полностью соответствует рыночным стандартам для позиции Директора по клинической разработке в районе залива Сан-Франциско (Bay Area), где ставки традиционно выше средних по США.

Сопроводительное письмо

I am writing to express my strong interest in the Director, Clinical Development position at Revolution Medicines. With over 8 years of experience in the biotechnology industry and a PhD in a relevant field, I have a proven track record of leading cross-functional teams through the complexities of early and late-stage oncology clinical trials. My expertise in developing Clinical Development Plans and overseeing protocol execution aligns perfectly with your mission to inhibit frontier targets in RAS-addicted cancers.

Throughout my career, I have successfully managed study start-ups, data interpretation, and regulatory document authoring, ensuring that clinical objectives are met with the highest standards of data quality. I am particularly drawn to Revolution Medicines' innovative approach to RAS(ON) inhibitors and am eager to contribute my strategic thinking and operational leadership to your high-energy R&D pipeline. I am confident that my collaborative leadership style and deep understanding of oncology clinical development will make me a valuable asset to your team.

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Откликнитесь в revolutionmedicines уже сейчас

Присоединяйтесь к команде Revolutionaries и возглавьте разработку инновационных методов лечения рака уже сегодня!

Описание вакансии

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

The Director, Clinical Development will contribute to the scientific, clinical, and operational scope of assigned study protocols. This role will work with the cross-functional teams for the design, execution, and monitoring of clinical studies, as well as oversee data review, interpretation, and communication to both internal and external stakeholders. Oncology and/or late-stage experience is preferred.

  • Develop and execute clinical development strategies and the Clinical Development Plan (CDP) with a focus on early-phase development.
  • Lead cross-functional teams with oversight from senior team members to conduct clinical studies, including study start up, execution and close out activities, data review/analysis, and preparation of study reports.
  • Oversee the development of program-level documents, including but not limited to clinical protocols, investigator’s brochure, clinical study reports, abstracts and manuscripts, presentations, and various other internal and external documents and communications as needed.
  • Conduct ongoing data reviews; prepare and present summaries to internal and external stakeholders.
  • Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety.
  • Interact with internal and external stakeholders (investigators, study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalation.
  • Conduct literature reviews as needed.
  • Travel: Up to 20%.

Required Skills, Experience and Education:

  • A PhD, PharmD or equivalent is required. The years of experience are based on clinical development or similar relevant experience.
  • Minimum 8+ years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or related role.
  • Proven leadership in a collaborative team setting and driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
  • Detail-oriented with ability prioritize tasks and function independently as appropriate.
  • Strong organizational skills and an ability to interpret, discuss, and report trial/program level data effectively and identify trends.
  • Proficient with software tools (Microsoft Office), Electronic Data Capture, and other custom web-based software.
  • Excellent written and verbal communication skills.

Preferred Skills:

  • Strong experience with clinical data review and data quality assurance.
  • Knowledge and experience with clinical trial management and oversight.
  • Understanding and experience in clinical trial protocol and regulatory document authoring.

#LI-Hybrid  #LI-SH1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.

Base Pay Salary Range

$211,000—$264,000 USD


We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.


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Навыки

  • Data Analysis
  • Project Management
  • Microsoft Office
  • Clinical Development
  • Clinical Trials
  • Regulatory Documentation
  • Clinical Data Review
  • Oncology Oncology
  • Electronic Data Capture

Возможные вопросы на собеседовании

Проверка стратегического мышления и понимания специфики компании.

Как бы вы адаптировали план клинической разработки (CDP) для ингибитора RAS(ON) с учетом конкурентной среды в прецизионной онкологии?

Оценка опыта работы с данными и принятия решений.

Опишите случай, когда в ходе мониторинга данных клинического исследования вы выявили критический тренд. Каковы были ваши действия?

Проверка лидерских качеств и навыков управления стейкхолдерами.

Как вы подходите к разрешению конфликтов между клиническими целями и операционными ограничениями при работе с кросс-функциональными командами?

Оценка опыта взаимодействия с регуляторами и подготовки документов.

Каков ваш опыт в подготовке брошюр исследователя (IB) и протоколов для подачи в регуляторные органы (например, FDA)?

Проверка готовности к специфике работы в биотех-стартапе/средней компании.

Как вы приоритизируете задачи в условиях высокой неопределенности и быстро меняющихся приоритетов в R&D пайплайне?

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Страна
США
Зарплата
211 000 $ – 264 000 $