研究设计专员
Study Design Specialist
CRIO（临床研究IO）是一家健康科技公司，帮助制药、生物技术、研究机构和学术研究中心通过一个系统和单一的临床数据采集来源，简化监管流程。我们的模块使机构能够实时电子化采集数据，为数据管理人员和监查员提供增强的透明度，并使申办方和CROs能够进行远程监查。
CRIO的eSource和CTMS系统是一个领先的现代企业级平台，专为临床研究机构设计。自2016年推出以来，CRIO在eSource领域建立了领先地位，并赢得了近50%的新兴企业级机构网络，其中许多机构得到了风险投资、私募股权和企业投资者的支持。CRIO实现了附带的指标，且几乎没有任何对外销售或营销活动。
研究设计专家负责在CRIO平台上从头到尾创建全面的研究构建。这包括根据方案和eCRF开发eSource，并进行构建后的质量控制审查。该职位将被视为CRIO eSource模块的行业专家。
**职责：**
- 利用方案、eCRF指南、药房手册、实验室手册和其他源文件为客户创建全面的构建。
- 完成客户要求的编辑和定制。
- 管理复杂的试验，确保所有数据都被正确采集。
- 修改标准模板以符合方案要求。
- 按时完成任务。
- 指导和培训现有及新入职的CRIO员工。
**优先资格：**
- 在CRIO或其他eSource/CTMS系统中具有eSource和QC设计经验。
- 医学或科学领域的学士学位。
- 具有研究协调员、机构负责人或源设计者的经验者优先。
**其他资格：**
- 至少1年的医疗保健行业经验。
- 能够解读临床试验方案和源文件。
- 熟悉医学术语和程序。
- 强大的人际沟通能力。
- 注重细节，具备良好的时间管理能力。
- 有条理，能够建立优先级并高效执行任务。
加入CRIO，成为一支致力于革新临床研究行业的动态团队的一员。立即申请，开启一段富有成就感的职业旅程！
**平等就业机会**
我们自豪地作为一家平等就业机会雇主，欢迎员工的多样性，无论其种族、性别、宗教、年龄、残疾或任何其他特征。
查看英文原文
CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture. Our modules allow sites to capture data electronically in real-time, providing data managers and monitors with enhanced transparency, and enabling remote monitoring by sponsors and CROs.
CRIO’s eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO’s launch in 2016, CRIO has established the leading brand position in eSource and has won close to 50% of the emerging class of enterprise-grade site networks, many of whom are backed by institutional investors such as VC, PE and corporations. CRIO has achieved the attached metrics, all with little to no serious outbound sales or marketing.
The Study Design Specialist is responsible for creating comprehensive study builds from start to finish in the CRIO platform. This includes developing eSource from protocols and eCRFs, and conducting post-build quality control reviews This individual will be considered an industry expert on the CRIO eSource module.
**Responsibilities:**
- Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients.
- Complete client-requested edits and customizations.
- Manage complex trials to ensure all data is captured appropriately.
- Modify standard templates to comply with protocol requirements.
- Complete assignments on time.
- Mentor and train current and new CRIO employees.
**Preferred Qualifications:**
- Experience with eSource and QC design in CRIO or other eSource/CTMS systems.
- BS in medical or sciences field.
- Experience as a Research Coordinator, Site Director, or Source Designer is a plus.
**Other Qualifications:**
- At least 1 year of healthcare experience.
- Ability to interpret clinical trial protocols, and source documents.
- Knowledge of medical terminology and procedures.
- Strong people skills.
- Detail-oriented with solid time management skills.
- Well-organized, capable of establishing priorities, and executing tasks efficiently.
Join us at CRIO and be part of a dynamic team dedicated to revolutionizing the clinical research industry. Apply today to embark on a rewarding career journey!
**Equal Employment Opportunity**
We’re proud to be an equal opportunity employer and welcome our employee’s differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Difference makes us better. Join us.
**Benefits**
This is a part time role:
Compensation Package - $20 an hour for all training and up to $450 for Study Design Build