
Clinical Research Operations Specialist
1 week ago
As a Clinical Trial Coordinator, you will play a critical role in the success of our clinical trials. You will be responsible for coordinating and facilitating project activities, serving as a study lead, and acting as a cross-functional liaison for the project team.
You will provide administrative and technical support to the Project Team, coordinate and facilitate project activities, and serve as a study lead. You will also act as a buddy during the onboarding phase and provide training to new staff as needed.
- Coordinate and oversee trial activities, ensuring timely completion and high-quality standards.
- Perform departmental and country file reviews, documenting findings in appropriate systems.
- Ensure allocated tasks are performed on time, within budget, and to a high standard.
- Proactively communicate any risks to project leads and line managers as appropriate.
**Required Skills and Qualifications**
- Bachelor's degree preferred.
- 4+ years of experience in a Clinical Trial Coordinator role.
- Experience with Veeva Vault, CTMS tools, and eTMF systems.
- Global clinical trials experience and supporting global project managers.
**Benefits**
- Ability to work independently or as part of a team.
- Strong organizational skills and attention to detail.
- Proven ability to handle multiple tasks efficiently and effectively.
- Excellent English language and grammar skills.
- Proficient local language skills (as needed).
**Others**
- Good presentation skills.
- Excellent computer skills (MS Office, Word, Excel, PowerPoint).
- Ability to obtain knowledge and master all clinical trial database systems.
- Self-motivated, positive attitude with effective interpersonal skills.
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