Experienced Clinical Research Associate - Multi-Sponsored Model

Youll have training and development to plan and progress your career in the direction you choose. And you wont do it alone you will have dedicated mentoring and receive structured quarterly reviews on performance promotion and bonus awards.

While Projects Vary Your Typical Responsibilities Might Include

• Performing site selection initiation monitoring and close-out visits plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions recruitment case report form (CRF) completion and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally you will also have a good basic knowledge of applicable clinical research regulatory requirements.


You Should Have

• A Bachelors degree in a health care or other scientific discipline or educational equivalent
• At least 15 - 2 years of on-site monitoring experience
• Fluent in Arabic and English language
• Good written and verbal communication skills including good command of English language
• Requires frequent travel to sites
• Flexible about location but location must have good connectivity to travel
• Homebased

If you want to make an impact in the global research market where we are working to make a real difference in patient health we ask you toapply now and join our team.
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