contract managementquality managementclinical researchcontract strategyclinical trialsctmsclinical site contracting
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше среднего
$87к-216к/год
$110к$130кмедиана$150к
По похожим ролям (50) ~ $130к/год
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Чётко описанная позиция senior-уровня в крупной компании клинических исследований с зарплатой примерно на уровне рынка, но широкий диапазон оставляет неопределённость по итоговому предложению.
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Широкий диапазонПонятные задачиКрупная компания
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Global Site Contract Manager (Clinical Research): Managing contract strategy and start-up contracting activities for complex clinical studies and multi-protocol programs with an accent on investigator grant estimates, site agreements, regulatory compliance, and cross-country coordination. Focus on developing contracting systems and templates, analyzing contracting intelligence, maintaining project timelines and financial goals, and mentoring colleagues.
Location: Durham, North Carolina, United States of America
Base pay: $86,500.00–$216,000.00 annualized
Company
hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
Manage contract strategy and start-up contracting activities for selected sponsors, complex studies, and multi-protocol programs.
Develop investigator grant estimates, contracting strategies, contract and budget templates, systems, tools, processes, and training materials.
Coordinate with sponsors, study stakeholders, regions, and countries to deliver project scope in compliance with sponsor requirements and management plans.
Provide legal, operational, and financial contracting support for site agreements and complex clinical trials.
Analyze contracting intelligence, report performance metrics, and maintain project timelines, plans, databases, and CTMS records.
Mentor colleagues, provide technical guidance, deliver presentations, and support long-term client relationships.
Requirements
Bachelor's degree.
5 years of relevant sponsor or clinical research organization clinical site contracting experience.
Demonstrable experience acting as an international contract expert.
Ability to support complex clinical trials while complying with regulatory requirements and local laws.
Experience collaborating with sponsors, stakeholders, study teams, and international regions and countries.
Culture & Benefits
Full-time employment.
Potential incentive plans, bonuses, and additional compensation may be available depending on the position.
Health and welfare benefits may be provided.
Equal opportunity employment environment.
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