- Страна
- США
- Зарплата
- 250 000 $ – 305 000 $
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Senior Director, Clinical Pharmacology
Исключительная позиция уровня Senior Director с высокой зарплатой, возможностью удаленной работы и неограниченным оплачиваемым отпуском. Компания находится на острие инноваций в иммунологии, что предлагает отличные карьерные перспективы.
Сложность вакансии
Высокая сложность обусловлена требованием 8-10 лет опыта, наличием ученой степени (PhD/MD) и успешным опытом прохождения регуляторных одобрений (NDA/BLA). Роль подразумевает руководство всей функцией клинической фармакологии в компании.
Анализ зарплаты
Предлагаемая зарплата ($250k - $305k) находится в верхнем дециле рынка для позиций Senior Director в биотехнологических компаниях США, особенно с учетом возможности удаленной работы. Суммарный пакет с опционами и бонусами делает это предложение крайне конкурентоспособным.
Сопроводительное письмо
I am writing to express my strong interest in the Senior Director, Clinical Pharmacology position at Immunovant. With over a decade of experience in drug development and a proven track record of leading successful regulatory submissions (NDAs/BLAs), I am confident in my ability to drive the clinical pharmacology strategy for your anti-FcRn pipeline. My expertise in PK/PD modeling, pharmacometrics, and cross-functional leadership aligns perfectly with Immunovant's mission to enable normal lives for people with autoimmune diseases.
Throughout my career, I have specialized in using modeling and simulation to accelerate development timelines and optimize dosing strategies. I am particularly drawn to Immunovant’s entrepreneurial environment and the opportunity to serve as the functional head of clinical pharmacology. I look forward to bringing my technical rigor and strategic vision to your dynamic team to help advance transformative therapies for patients in need.
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Присоединяйтесь к лидеру в области иммунологии и возглавьте стратегию клинической фармакологии для инновационных методов лечения!
Описание вакансии
Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.
The Role:
The Senior Director, Clinical Pharmacology is responsible for developing clinical pharmacology plans and overseeing the execution of these plans across therapeutic areas and in all phases of clinical development. This leadership role will have direct reports and is an integral member of the project team and serves as the clinical pharmacology and pharmacometrics lead for individual asset(s). This person designs and interprets clinical pharmacology studies and writes relevant sections of regulatory documents, protocols, and study reports. They use exploratory data analyses techniques, modeling, and simulations to accelerate development and support dosing, study designs, and development plans. They perform pharmacometrics analyses or provide scientific oversight of pharmacometrics analyses performed by external resources.
Key Responsibilities:
- Serve as the head of clinical pharmacology and leader of the function for all indications
- Develop clinical pharmacology strategy for all Immunovant compounds and design, interpret, and conduct clinical pharmacology studies
- Provide clinical pharmacology support for Ph 1, 2, and 3 studies
- Support clinical pharmacology aspects of regulatory submissions including writing and review of relevant sections
- Provide data analyses, modeling and simulation to support asset development; perform pharmacometrics analyses or provide scientific oversight of pharmacometrics analyses performed by external resources.
- Collaborate closely with Regulatory to provide CP support of regulatory documents, communications, and presentations as needed (IND, health authority inquires, preparation/participation in meetings with health authorities, preparation of relevant BLA sections, addressing review inquiries, health authority sponsored Advisory Committee Meetings).
- Support cross-functional teams, including Statistics, Data Management, Clinical, Preclinical/Nonclinical, Translational Science, as needed.
Requirements:
- PhD, PharmD, or MD with training in CP, PK/PD, Pharmacology, and Pharmaceutical Sciences.
- 8-10 years of experience in the application of CP within the context of drug development in the healthcare industry.
- Experience in leadership of CP regulatory submission and approvals of at least one original or major NDA/CTDs or multiple supplemental NDA/CTDs (global or regional)
- Proven track record of clinical pharmacology and pharmacokinetic / pharmacometrics support for regulatory submissions (e.g., EoP2, IND, NDA, MAA, PIP)
- Experience and expertise with pharmacokinetics / pharmacometrics methods and software (e.g, NONMEM, WinNonlin)
- Deep understanding of drug development and the integration across the various functions including nonclinical, clinical, CMC, regulatory, finance and legal.
- Knowledge of regulatory expectations for clinical pharmacology
- Excellent written and oral communication skills with meticulous attention to detail.
- Thrives in a dynamic, interactive, fast-paced, innovative, and entrepreneurial environment.
- Natural collaborator who enjoys working on a cross-functional team.
Work Environment:
- Immunovant’s headquarters is located in New York City. The position is flexible for remote work.
- Dynamic, interactive, fast-paced, and entrepreneurial environment
- Domestic or international travel may be required (<10%).
Salary range for posting
$250,000—$305,000 USD
Compensation is based on a number of factors, including market location, and may vary depending on job-related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.
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Навыки
- Clinical Pharmacology
- Pharmacometrics
- Pharmacokinetics
- Pharmacodynamics
- NONMEM
- WinNonlin
- Regulatory Submissions
- Drug Development
- Modeling and Simulation
Возможные вопросы на собеседовании
Проверка опыта взаимодействия с регуляторами на высоком уровне.
Опишите ваш опыт подготовки разделов клинической фармакологии для BLA/NDA и защиты стратегии перед FDA или EMA.
Оценка навыков стратегического планирования в разработке лекарств.
Как вы используете моделирование и симуляцию (M&S) для оптимизации дизайна исследований 2-й и 3-й фаз?
Проверка лидерских качеств и умения управлять командой.
Расскажите о вашем подходе к руководству прямыми подчиненными и управлению внешними ресурсами (CRO) в области фармакометрики.
Оценка способности работать в междисциплинарной среде.
Как вы обеспечиваете интеграцию данных клинической фармакологии с отделами доклинических исследований, CMC и клиники?
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Каков ваш опыт работы с моноклональными антителами или технологиями anti-FcRn в контексте фармакокинетики?
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- Страна
- США
- Зарплата
- 250 000 $ – 305 000 $