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1 week ago
This is a key role in the management of clinical studies. The position involves overseeing project operations, site selection and initiation, study monitoring and close-out. It requires strong organizational skills, knowledge of regulatory requirements and ability to work independently.
Main Responsibilities:- Study Site Selection and Initiation: Identify and evaluate potential study sites, ensure they meet sponsor criteria and facilitate timely initiation of studies.
- Project Management: Oversee study activities, track progress, identify issues and implement corrective actions to meet project timelines.
- Study Monitoring: Conduct on-site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and applicable regulations, address site issues and maintain accurate records.
Key Qualifications:
- Bachelor's degree in a related field, such as medical, pharmacology or biology.
- Minimum 3 years' experience in clinical research associate roles.
- Strong understanding of GCP principles and clinical trial processes.
- Excellent communication and organizational skills.
This opportunity offers a chance to work on high-profile clinical studies, develop your skills and expertise in clinical research and contribute to the success of our organization. If you are motivated, organized and have a passion for clinical research, we encourage you to apply.
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