
Clinical Research Associate Position
2 weeks ago
We are seeking a highly skilled Clinical Research Associate to join our team. In this role, you will be responsible for conducting site qualification, site initiation, interim monitoring, and site management activities at investigator/physician sites.
Key Responsibilities:
- Perform site qualification, site initiation, interim monitoring, and site management activities to ensure regulatory compliance.
- Evaluate overall performance of sites and provide recommendations for site-specific actions.
- Maintain knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes.
- Verify informed consent processes and assess factors that might affect subject/patient safety and clinical data integrity.
- Conduct source document reviews, verify clinical data accuracy, and apply query resolution techniques.
- Perform investigational product inventory, reconciliation, and reviews storage and security.
Requirements:
- Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience.
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
- Excellent communication, presentation, and interpersonal skills.
- Ability to manage required travel of up to 75% on a regular basis.
About Us:
We are committed to building a diverse, inclusive, and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway.
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