
Clinical Research Associate
Há 22 horas
We are seeking a skilled and experienced Clinical Research Associate to oversee clinical trials and ensure the highest standards of quality and safety.
Key Responsibilities:
- Evaluate study sites for compliance with established protocols and regulatory guidelines.
- Conduct site visits to assess the effectiveness and safety of investigational products and medical devices.
- Coordinate clinical monitoring processes in accordance with industry regulations and company policies.
Requirements:
- Bachelor's degree in a relevant scientific field such as life sciences or public health.
- At least five years of experience in clinical operations, preferably in oncology global trials.
- Excellent communication, interpersonal, and organizational skills.
- Prior experience in data management systems and CTMS software is preferred.
Preferred Qualifications:
- Fluent English language skills (speaking and writing).
- Proficient in Microsoft Office applications including Word, Excel, PowerPoint, and Outlook.
- Familiarity with electronic document management systems and other industry software.
Travel:
Up to 70% travel may be required for this role, which includes regular site visits and meetings with research teams.
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