regulatory affairsoncologyclinical researchdrug developmentcross functional teamworkhematologyclinical trialsbiomedical research
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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$256к-403к/год
$150к$240кмедиана$280к
По похожим ролям (50) ~ $240к/год
90
Крутая вакансия
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В Company hidden чётко описана руководящая роль в клинических исследованиях по гематологии с участием в разных этапах разработки препаратов и хорошим пакетом льгот; вакансия доступна только жителям США и Пуэрто-Рико.
Только США и Пуэрто-Рико
Понятная зона ответственности
Крупная фармкомпания
Широкий пакет льгот
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Director, Clinical Research, Hematology (Oncology): Planning and directing clinical research for investigational and marketed medicines across the development lifecycle with an accent on hematology, clinical trial oversight, and scientific evaluation. Focus on designing and executing trials, analyzing safety and efficacy findings, coordinating cross-functional development teams, and supporting regulatory submissions and publications.
Location: United States and Puerto Rico residents only; primary location: Rahway, New Jersey. Flexible work arrangements: Remote. Travel approximately 20% of the time.
Base salary: $255,800–$402,700 annually for the primary location; annual bonus and long-term incentive may also apply.
Company
hirify.global develops investigational and marketed medicines across oncology and other therapeutic areas.
What you will do
Plan clinical trials and collaborate on operational plans based on clinical development strategy.
Provide medical oversight for ongoing and new trials involving investigational or marketed drugs.
Analyze and summarize clinical findings to support safety and efficacy decisions, regulatory submissions, clinical study reports, and publications.
Coordinate with commercialization, regulatory affairs, statistics, manufacturing, and other functional experts on clinical development projects.
Identify and communicate with clinical investigators, maintain scientific knowledge, and provide internal and external scientific expertise.
Author development documents, presentations, budgets, and position papers; facilitate external research collaborations.
Requirements
M.D. or M.D./Ph.D.
Experience in industry or as senior faculty in academia.
At least 3 years of clinical medicine experience.
At least 1 year of industry experience in drug development or biomedical research experience in academia.
Demonstrated scientific scholarship and achievement, with a proven track record in clinical medicine and biomedical research.
Strong interpersonal skills and the ability to work effectively in a team environment.
Strong verbal, written communication, and presentation skills.
Required expertise includes clinical investigations, clinical research, clinical trial planning and support, clinical judgment, biomedical research, regulatory requirements, scientific consulting, academic presentations, cross-functional teamwork, adaptability, ethical standards, intellectual curiosity, and new technology integration.
Nice to have
Board certification or eligibility in oncology, hematology, or a related discipline.
Prior specific clinical research experience and prior publication experience.
Culture & Benefits
Remote flexible work arrangement with approximately 20% business travel.
Medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including a 401(k), paid holidays, vacation, compassionate leave, and sick days.
Inclusive environment that values diverse experiences and perspectives and encourages respectful challenge and collaborative problem-solving.
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