- 经验
- 1年以上
- 薪水
- —
- 职位空缺
- 1
- 发布
- 2周前
- 工作模式
- 在家办公
- 学历
- 学士学位
- 合格
- Candidates with a relevant bachelor's degree and at least 1.5 years of clinical research experience, especially in pharma or biotech, are suitable for this role.
- 恢复
- 需要申请
职位描述
Role overview
This opening is for a full-time remote Clinical Research Associate role supporting sponsor-dedicated studies. The selected professional will help run and coordinate clinical trials while making sure all activities align with applicable regulatory standards. A major part of the job is maintaining precise, complete study documentation and working in sync with the wider clinical research team to support trial delivery.
Qualifications
- A bachelor's degree in a relevant discipline, such as Life Sciences, Nursing, or another science-focused field.
- At least 1.5 years of experience in clinical research, preferably gained in a pharma or biotech environment.
- Working knowledge of ICH/GCP and FDA regulations, along with exposure to protocol development and study start-up.
- Strong organizational abilities and clear communication skills.
- Ability to perform effectively both independently and as part of a team.
- Good working knowledge of Microsoft Office tools, including Word, Excel, and PowerPoint.
- Prior use of clinical trial systems such as EDC and IWRS would be an advantage.
- Background in oncology or other therapeutic areas would be a plus.
- Strong problem-solving capability and sound decision-making skills.
Application note
Candidates were asked to send their CV to [email protected].