data analysisregulatory affairsclinical researchdrug developmenthematologyclinical trialsbiomedical researchclinical developmentclinical medicine
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
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$282к-444к/год
$190к$260кмедиана$290к
По похожим ролям (50) ~ $260к/год
90
Крутая вакансия
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В Company hidden это четко очерченная руководящая роль в клинических исследованиях гематологических препаратов, с участием во всем цикле разработки в крупной фармацевтической компании.
?Высокий уровень ответственности
Крупная фармкомпания
Влияние на лечение
?Поездки по работе
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Director, Clinical Research, Hematology (Clinical Development/Drug Development): Planning and directing clinical research for investigational and marketed hematology medicines across the clinical development cycle with an accent on study design, medical oversight, clinical analysis, regulatory reporting, and publication. Focus on evaluating translational research, developing clinical strategies, overseeing trials, collaborating with regulatory, statistical, manufacturing, and commercialization experts, and supporting complex drug development decisions.
Location: Hybrid; primary location in Rahway, New Jersey, USA. This role is available to US and Puerto Rico residents only.
Base salary: $282,200–$444,200 per year for the primary location; annual bonus and long-term incentive may also apply.
Company
hirify.global develops and researches medicines, including oncology products across pre-clinical, clinical, and post-licensure stages.
What you will do
Plan and direct clinical research for investigational and marketed hematology medicines across study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.
Evaluate pre-clinical and translational research, develop early clinical development plans, and support Investigational New Drug applications.
Develop clinical strategies and plan trials in collaboration with operational teams.
Provide medical oversight for ongoing and new clinical trials and analyze findings for safety, efficacy, regulatory submissions, clinical study reports, and publications.
Collaborate with internal and external research teams, investigators, regulatory affairs, statistics, manufacturing, and commercialization functions.
Prepare development documents, presentations, budgets, and position papers; facilitate external research collaborations and travel approximately 20% for clinical research projects.
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 and at least 3 years of industry experience in drug development or biomedical research experience in academia.
Demonstrated success overseeing clinical studies and protocols, with a record of scientific scholarship and achievement.
Proven clinical medicine track record and a biomedical research background.
Strong interpersonal skills and ability to work in a team environment.
Outstanding verbal and written communication and presentation skills.
Nice to have
Board certification or eligibility in oncology, hematology, or a related discipline.
Specific prior clinical research experience and prior publications.
Culture & Benefits
Hybrid work arrangement with regular collaboration across functional and external research groups.
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 perspectives, respectful challenge, and collective problem solving.
Hiring process
Applications are accepted through the hirify.global careers portal; current employees and contingent workers use the designated internal application routes.
Accommodation support is available during the hiring process for US and Puerto Rico residents.
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