CareerOpportunitiesInClinicalResearch

Clinical Research Associate

As a clinical research professional, you will have the opportunity to launch your career in a structured and accredited environment.

The role involves assisting with on-site coordination of clinical trial activities, maintaining essential documents, and ensuring compliance with ICH-GCP and ethical guidelines. This requires attention to detail, effective communication skills, and the ability to work independently as part of a team.

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• Assist with on-site coordination of clinical trial activities under supervision, including scheduling site visits, managing documentation, and communicating with stakeholders">
• Maintain accurate and up-to-date records, case report forms, and site files, adhering to regulatory requirements and company policies">
• Support investigators in protocol compliance and patient coordination, providing guidance and resources as needed">
• Ensure all trial activities adhere to ICH-GCP and ethical guidelines, identifying and mitigating potential risks and issues">
• Participate in training sessions and team meetings to enhance knowledge and skills, staying current with industry developments and best practices">

To be eligible for this role, you should possess a strong background in life sciences or pharmacy, with excellent communication and organizational skills. A willingness to learn and grow in the clinical research domain is essential.

We offer a supportive and collaborative environment that fosters growth and development, allowing you to work alongside expert mentors and gain practical exposure.