
Clinical Research Associate
1 day ago
As a Clinical Research Associate, you will play a crucial role in ensuring the accuracy and quality of clinical trial data. Your responsibility will be to conduct site visits, monitor trial conduct, and maintain compliance with regulatory requirements.
Key Responsibilities:
- Evaluate site performance, identify potential issues, and recommend corrective actions.
- Conduct source document review and verification to ensure data integrity.
- Manage protocol deviations, ensure timely reporting, and facilitate resolution.
Required Skills and Qualifications:
- 3+ years of experience in clinical monitoring or research coordination.
- Effective communication and interpersonal skills.
- Ability to work independently and as part of a team.
Benefits:
- Opportunity to contribute to a dynamic and ambitious team.
- Professional growth and development opportunities.
- Collaborative and inclusive work environment.
Our Company Culture:
We value innovation, teamwork, and employee growth. Our mission is to improve patient outcomes through high-quality clinical trials.
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