M
- 経験
- どれでも
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 3時間前
- 作業モード
- 在任中
- 教育
- 高校卒業証書
- 再開する
- 応募必須
勤務地
仕事内容
Position Summary
This role supports clinical research coordinators or nurses by handling various administrative duties and assisting with study documentation to ensure compliance with protocols and regulations.
Key Responsibilities
- Providing administrative support including organizing processes, managing study materials, and data entry tasks.
- Maintaining well-organized files, logs, and related documentation efficiently.
- Helping clinical research staff document study requirements in line with internal and external standards.
- Updating systems used for clinical trial management.
- Ensuring clinical trial documents are signed and submitted within required timelines.
- Engaging in mentorship for skill enhancement following initial orientation.
- Handling assignments based on one's skills and experience, with opportunities to take on more complex tasks independently.
- Responding promptly to requests from internal and external stakeholders.
- Assisting in coordinating visits from study sponsors.
- Conducting data quality checks as necessary.
- Performing additional related duties as assigned.
Qualifications
- Must possess a high school diploma.
- Preferred experience includes at least six months of data entry and prior office experience in a medical environment.
Additional Information
- Work schedule is part-time, from 8:00 AM to 4:30 PM.
- Total work hours per pay period amount to 80.
- The position does not require weekend or on-call duties.
- Requisition ID: 26003640.