Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Малоразвернуть
$72к-88к/год
$95к$120кмедиана$140к
По похожим ролям (49) ~ $120к/год
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Обязанности описаны понятно, а зарплата указана открыто, но оплата ниже медианы рынка, и иногда могут требоваться дополнительные часы.
Оплата ниже рынка
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Research Admin Specialist II-CTMS (OnCore) (Clinical Research/CTMS): Developing clinical trial calendars, financial consoles, coverage analyses, budgets, and regulatory documentation for multiple clients with an accent on clinical research administration, CTMS configuration, and guideline interpretation. Focus on building accurate trial deliverables, applying Medicare and FDA requirements, and supporting quality assurance and client-specific research operations.
Location: Full-time US-REMOTE role; U.S. work authorization required. The posting also lists Chicago - 550 Van Buren.
Base salary: $72,000–$88,000 annually; total estimated compensation including annual incentive opportunity: $79,200–$96,800.
Company
hirify.global collaborates with higher education organizations and academic medical centers on organizational effectiveness, student outcomes, technology implementation, and sustainable funding.
What you will do
Develop CTMS calendars for multiple clients, including arms, segments, procedures, and visit assignments.
Build financial consoles for new and legacy clinical trials, including protocol elements, parameters, specifications, subject-related items, and milestones.
Develop coverage analyses in Excel and client CTMS platforms.
Create research administration deliverables, including budgets, budget negotiations, sponsor invoicing, accounts receivable management and reconciliation, and regulatory administrative support.
Review and provide feedback on Research Administrative Specialist I projects and begin supporting client-specific contacts and needs.
Requirements
U.S. work authorization is required.
Bachelor’s degree in a health- or science-related discipline, such as biology, public health, healthcare administration, or nursing, or equivalent professional experience.
At least 3 years of clinical research administration experience, including exposure to coverage analysis, clinical trial budgeting, and/or CTMS calendar or financial console development.
Ability to interpret and apply clinical guidelines from the Centers for Medicare and Medicaid, the Food and Drug Administration, and the National Comprehensive Cancer Network.
Strong attention to detail and ability to produce quality-assured research back-office deliverables with minimal to no errors.
Intermediate Excel competency.
Full-time salaried work; additional hours may be required based on business needs.
Nice to have
Experience with Forte Research System’s OnCore, Study Manager’s Reveal, Velos’s eResearch, or Patient Protocol Manager.
Experience conducting quality assurance reviews.
Experience developing others and training new skills.
Experience drafting standard operating procedures or other process documents.
Culture & Benefits
Remote work arrangement for a full-time U.S.-based role.
Eligibility for hirify.global’s annual incentive compensation program.
Medical, dental, and vision coverage.
Additional wellness programs and benefit plans.
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