临床研究支持
Clinical Research Support
职位描述
岗位职责：
我们正在寻找一位临床研究支持专业人员，协助研究启动、合同和预算、患者随访协调，并确保患者在整个研究参与过程中有良好的体验。该职位将远程协助站点经理完成日常临床研究任务。该职位的目标是提供可靠且高效的行政和研究支持，加快任务完成速度，提高周转效率，并优化研究站点的整体工作流程。
主要职责：
• 患者随访协调和安排
• IRB提交及相关监管文件（电子源文件）
• 供应商和设施协调
• 预算谈判和跟进
• 合同协调和跟踪
• ICF（知情同意书）文件和管理
• 研究启动支持
• 维护和整理研究文件
• 跟进未完成的任务并确保按时完成
所需技能/经验：
该职位需要对临床研究流程和过程有深入了解，包括IRB提交、知情同意书（ICFs）、纸质源文件、预算和合同。被选中的候选人还将支持站点向eSource系统的过渡，预计将在未来三个月内完成。我们目前的站点日常运营使用Google Workspace（G Suite）和Microsoft工具，因此熟悉这些工具是优先考虑的。
不可妥协的要求（硬性条件）：
• 认真细致，注重细节，能够持续跟进分配的任务。
• VA应具备扎实的临床研究流程知识，并能独立工作，同时确保任务准确且按时完成。
• 强烈的责任感、组织能力和主动沟通至关重要
工具/系统与合规：
Google Workspace（G Suite）
Microsoft Tools
优先考虑会说西班牙语的候选人
最初发布于Himalayas
查看英文原文
Job Description
Role Purpose:
We are looking for a Clinical Research Support professional to assist with study start-ups, contracts
and budgets, patient visit coordination, and ensuring a positive patient experience throughout study participation.
This position will provide additional support to the Site Manager, by assisting with day-to-day clinical research tasks remotely. The goal of the role is to provide reliable and efficient administrative and research support, help complete tasks more quickly, improve turnaround times, and streamline the overall workflow of the research site.
Key Responsibilities:
• Patient visit coordination and scheduling
• IRB submissions and related regulatory documentation (electronic source)
• Vendor and facility coordination
• Budget negotiation and follow-up
- Contract coordination and tracking
- • ICF (Informed Consent Form) documentation and management
- • Study start-up support
- • Maintaining and organizing study documentation
- • Following up on outstanding tasks and ensuring items are completed on time
Required Skills / Experience:
The role requires a strong understanding of clinical research workflows and processes, including IRB submissions, informed consent forms (ICFs), paper source documentation, budgets, and contracts. The selected candidate will also support the site as it transitions to an eSource system, which is expected to take place within the next three months. Our site currently uses Google Workspace (G Suite) and Microsoft Tools for its day-to-day operations, so familiarity with these tools is preferred.
Non-Negotiables (Hard Requirements):
• Diligent, detail-oriented, and consistent in following through on assigned tasks.
• VA should have a solid understanding of clinical research processes and be able to work independently
while ensuring tasks are completed accurately and on time.
• Strong accountability, organization, and proactive communication are essential
Tools / Systems & Compliance:
Google Workspace (G Suite)
Microsoft Tools
Preferably Spanish speaking candidates
Originally posted on Himalayas