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Clinical Research Coordinator
1 week ago
At Monitoring Force, we don't just conduct clinical research, we work with sponsors to propose the project that meets their needs. Our expertise goes beyond conducting studies and focuses on proposing the right study. Our key figures reflect our global experience and diverse expertise. The story of our development during these last 20 years explains our unwavering commitment to meeting the unique needs of the GCC region. We're more than a CRO – we're a trusted partner, committed to delivering the project that meets your objectives, and results that exceed expectations. With us, your project is in the hands of leading experts who understand your challenges and share your goals.
About Monitoring Force: Join Monitoring Force, a pioneering Clinical Research Organization (CRO) committed to delivering diverse interventions for clinical research stakeholders, including pharmaceuticals, biotechs, and public institutions. Our expertise encompasses the initiation and monitoring of registration studies, project management, and analysis. As a group of companies, we lead projects in France, Europe, the Maghreb, and the Middle East. Our services include comprehensive clinical study management (Phases Ib to IV), pharmacoeconomic studies and observatories, data management and statistics, medical development consulting, and medical writing.
Clinical Research Coordinator | Monitoring Force Gulf Dubai | Apply Now
Do miss out on thisn't m exciting opportunity – apply now at
Key Responsibilities:
Lead and manage clinical trials (Phases Ib to IV) in Dubai, Saudi Arabia, and the broader GCC region, ensuring compliance with regulations.
Act as the primary liaison with investigators, healthcare professionals, hospital administration, and regulatory bodies.
Engage in comprehensive risk management for projects, identifying and addressing potential challenges.
Adhere to the General Data Protection Regulation (GDPR) standards in all activities.
Ensure compliance with internal policies, procedures, and work instructions relevant to the role.
Candidate Profile:
Educational Background: Bachelor's degree (or equivalent) in a scientific field, plus Clinical Research Associate training.
Language Skills: Fluent in English (essential) and Arabic (for Saudi Arabian projects). French proficiency is a plus, given our French roots and collaboration with headquarters.
Professional Skills: Proven expertise in clinical study regulations, medical terminology, therapeutic trials, medical English, and data collection/processing.
Personal Qualities: Methodical, adaptable, exceptional in cross-network collaboration, and superior communication skills.
What We Offer:
An opportunity to manage projects across Dubai, Saudi Arabia, and the GCC region.
A dynamic and innovative work environment that fosters teamwork and creativity.
A role in a globally-oriented company, blending international expertise with local insights.
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