
Senior Clinical Trial Coordinator
Há 5 horas
We are seeking a skilled Contract Clinical Trial Associate to contribute to our clinical trials team. As a key member of our team, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Key Responsibilities- Coordinate and administer clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials, such as informed consent forms and case report forms.
- Facilitate communication among cross-functional teams to ensure smooth trial execution.
- Contribute to the tracking and reporting of clinical trial metrics and milestones.
- Bachelor's degree in a scientific or healthcare-related field.
- Prior experience with ethics submissions (CEP/CONEP).
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with attention to detail.
- Good level of English.
We offer a range of benefits to support your well-being and work-life balance, including opportunities for growth and development.
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