
Clinical Trial Coordinator
16 hours ago
The role of a Clinical Research Associate (CRA) is crucial in ensuring the rights and well-being of trial participants are protected, while also guaranteeing that reported trial data are accurate, complete, and verifiable from source documents.
Key Responsibilities:
- Establish and maintain strong relationships with Principal Investigators, study coordinators, pharmacists, and site trial personnel to ensure trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Standard Operating Procedures (SOPs).
- Collaborate with colleagues to prepare site essential documents and support ethics and regulatory submission and approval processes.
- Monitor investigational sites per ICH GCP across all phases of a clinical trial, ensuring compliance with established protocols.
Requirements:
- Graduate degree in a clinical or life sciences-related field.
- Excellent time management, attention to detail, and ability to work effectively in a team environment.
- Minimum 6 months of independent CRA monitoring experience, dependent on job level.
What We Offer:
Our organization is committed to providing an inclusive work environment and promoting gender equality. We offer flexible working options, parental leave, wellness programs, and ongoing development opportunities to support our employees' growth and well-being.
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