2 дня назад
Research Admin Specialist II-CTMS (OnCore)
72 000 - 88 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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 research clients with an accent on clinical trial administration, CTMS configuration, and financial accuracy. Focus on interpreting clinical guidelines, building complex trial deliverables in OnCore and Excel, and performing quality assurance with minimal errors.
Location: US remote; U.S. work authorization required. The role is associated with Chicago, Illinois.
Salary: $72,000–$88,000 base annually, with total estimated compensation of $79,200–$96,800 including annual incentive compensation.
Company
helps higher education organizations and academic medical centers improve organizational effectiveness, implement technologies, align resources, and achieve sustainable growth.
What you will do
- Develop clinical trial calendars with arms, segments, procedures, and visit assignments in CTMS platforms.
- Build financial consoles with protocol elements, parameters, subject-related items, and milestones for new and legacy clinical trials.
- Develop coverage analyses in Excel and client CTMS systems for multiple research clients.
- Create research administration deliverables, including study budgets, sponsor invoicing, accounts receivable reconciliation, and regulatory support.
- Review projects completed by Clinical Research Administrative Specialist I staff and support client-specific needs.
Requirements
- U.S. work authorization is required.
- Bachelor’s degree in a health or science-related discipline, or equivalent professional experience.
- At least three years of clinical research administration experience, including coverage analysis, clinical trial budgeting, or CTMS calendar and financial console development.
- Ability to interpret and apply clinical guidelines from CMS, the FDA, and the National Comprehensive Cancer Network.
- Strong attention to detail and the ability to produce accurate research administration deliverables with minimal errors.
- Intermediate Excel competency.
Nice to have
- Experience with Forte Research System’s OnCore, Study Manager’s Reveal, Velos’s eResearch, or Patient Protocol Manager.
- Quality assurance review experience.
- Experience training others or developing standard operating procedures and process documents.
Culture & Benefits
- Full-time salaried US-remote work arrangement.
- Additional hours may be required depending on business needs.
- Eligibility for ’s annual incentive compensation program.
- Medical, dental, vision, and other wellness benefits.
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