Clinical Research Associate
hace 6 horas
We are seeking a highly skilled Clinical Research Associate to join our team of professionals in this key role. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials across various therapeutic areas.
The ideal candidate will possess excellent communication skills, attention to detail, and the ability to work effectively in a fast-paced environment. A strong understanding of Good Clinical Practice (GCP) regulations and clinical trial methodologies is essential for success in this position.
Responsibilities- Study Monitoring: Conduct site initiation visits, interim visits, and close-out visits to ensure compliance with study protocols and GCP regulations.
- Data Review: Verify and validate clinical trial data through source document verification and query management.
- Site Management: Identify and resolve site-related issues, provide support to sites, and maintain open lines of communication.
- Regulatory Compliance: Ensure adherence to regulatory requirements, including ICH-GCP guidelines and local regulations.
- Education: Bachelor's degree in a life science or a related field.
- Experience: Minimum 1-3 years of experience in clinical research, preferably as a CRA.
- Skills: Excellent communication and interpersonal skills, attention to detail, and ability to work effectively in a team environment.
- Knowledge: Strong understanding of GCP regulations, clinical trial methodologies, and regulatory requirements.
We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development in a dynamic and collaborative environment. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.
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