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Há 7 dias
As a Clinical Research Associate, you will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data.
Responsibilities Include:- Coordinate activities for setting up and monitoring studies, complete accurate study status reports, and maintain documentation.
- Run sponsor-generated queries efficiently and take responsibility for study cost efficiency.
- Develop strong relationships with stakeholders, investigators, and site staff.
- Ensure patient safety by adhering to procedures, protocols, and regulatory requirements.
- Bachelor's degree in health, life sciences, or related fields.
- Experience as CRA and on-site monitoring activities, preferably with medical device studies.
- Knowledge of ICH-GCP guidelines and expertise to review and evaluate medical data.
- Excellent written and verbal communication skills.
We offer competitive salaries and benefits focused on well-being and work-life balance. We prioritize diversity and inclusion and provide an accessible environment for all candidates.
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