Clinical Support Specialist (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Clinical Support Specialist (Clinical Research): Delivering clinical trial advancements for patients globally with an accent on site start-up activities, regulatory document management, and investigator recruitment. Focus on managing eTMF deliverables, coordinating Central EC applications, and ensuring timely site activation.
Location: Chicago, Illinois, United States
Company
specializes in precision medicine and the execution of targeted, adaptive clinical trials, primarily focused on oncology.
What you will do
- Support feasibility and investigator recruitment efforts for clinical trials.
- Drive site start-up activities, including milestone planning and managing submission/approval timelines.
- Review, validate, track, and file essential documents for investigational sites.
- Prepare and submit Central EC applications and support Local EC or hospital approval submissions.
- Maintain ownership of eTMF (Electronic Trial Master File) and manage study mailboxes.
- Provide administrative support, including team training maintenance, vendor coordination, and meeting minutes.
Requirements
- Secondary education or equivalent degree.
- 6 months to 6 years of experience in clinical research.
- Proficiency in Microsoft Office package (Outlook, Word, Excel, and PowerPoint).
- English: Professional level proficiency required.
- Location: Ability to travel domestically and internationally, including overnight stays.
Culture & Benefits
- Collaborative, close-knit team environment passionate about saving patients' lives.
- Culture centered around individual growth, career development, and professional balance.
- Environment where every voice matters and contributes to client goals.
- Equal Opportunity Employer commitment.
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