About the role

We are seeking a motivated Junior Clinical Research Associate to join our Franco-Saudi CRO team in an exciting international hybrid position. You’ll supervise a multi-center clinical study across 3 leading hospitals in the United Arab Emirates, while collaborating daily with our Paris-based senior CRA team who will provide structured mentorship and ongoing support.

This is an ideal opportunity for early-career clinical research professionals with GCP certification and 1-2 years of CRC or monitoring experience who are eager to rapidly develop expertise in international clinical trial monitoring through hands-on fieldwork, remote operations, and direct coaching from experienced European CRAs.

This is NOT a traditional office-based role. You’ll operate as an agile, international clinical research professional – working remotely from Saudi Arabia between monthly monitoring trips to UAE hospital sites, with continuous guidance from our Paris headquarters.

Key responsibilities

Clinical Site Monitoring (UAE Hospitals)

• Conduct regular monitoring visits to 3 hospital sites in UAE (4-6 days per month on-site)
• Perform Source Data Verification (SDV) ensuring data accuracy and protocol compliance
• Review informed consent processes, regulatory documentation, and essential files
• Build collaborative relationships with Principal Investigators and site coordinators

Data Quality & Compliance

• Manage and resolve EDC queries in collaboration with site teams
• Ensure adherence to ICH-GCP guidelines, study protocol, and SOPs
• Identify and report protocol deviations promptly
• Support Serious Adverse Event (SAE) reporting per regulatory requirements

Remote Operations & Reporting

• Work remotely from Saudi Arabia between site visits, managing follow-ups and documentation
• Prepare detailed monitoring visit reports for review by Paris senior team
• Participate in weekly video debriefings with Paris headquarters (collaborative learning)
• Maintain regular communication with sites via email, phone, and virtual meetings

Continuous Professional Development

• Receive structured training and mentorship from Paris-based senior CRAs (10+ years experience)
• Participate in international CRA best practices sessions (remote workshops)
• Develop expertise in multi-country regulatory frameworks (SFDA, MOHAP/DHA, ICH)

Required qualifications

Education & Certifications:

• Bachelor’s degree (minimum) in Life Sciences, Pharmacy, Nursing, Medicine, or related health field
• Valid GCP Certification (ICH-GCP) – MANDATORY and must be current
• Understanding of clinical trial lifecycle and ICH-GCP principles

Experience:

• 1-2 years in clinical research environment (CRC, junior CRA, hospital pharmacy with trial exposure, or clinical data management)
• Hands-on experience with Electronic Data Capture (EDC) systems (Medidata Rave, Oracle InForm, REDCap, or similar)
• Demonstrated understanding of monitoring activities (SDV, query management, regulatory documentation)

Language:

• Fluent English (written and spoken) – MANDATORY for UAE hospital interactions and Paris team collaboration
• Arabic proficiency is a plus

Practical Requirements:

• Valid passport with ability to travel regularly to UAE
• Comfortable with hybrid work model: remote work + monthly travel (4-6 days/month)
• Self-organized and disciplined for remote work environment
• Available to start within 30 days

Legal requirement:

• Saudi national (required for SFDA regulatory compliance)

What we’re looking for

Beyond technical qualifications, we value:

• International mindset who thrives in multi-cultural collaboration (French HQ, Saudi base, UAE sites)
• Self-motivated professionals comfortable working independently with remote guidance
• Quality-driven individuals who understand that rigorous data verification protects patient safety
• Strong communicators who can build bridges between investigators, sponsors, and internal teams
• Fast learners eager to absorb CRA best practices from experienced European mentors
• Adaptable problem-solvers who navigate challenges (site delays, travel logistics) with creativity
• Career-oriented professionals who see this as a launchpad to Senior CRA and beyond

What we offer

Professional Development:

• Intensive training and structured mentorship from experienced Parisian CRA team
• Weekly coaching sessions with Paris senior CRAs (10+ years expertise)
• Exposure to multi-country regulatory frameworks (SFDA + MOHAP/DHA + ICH)
• Access to advanced GCP courses and therapeutic area training
• Clear progression path: Junior CRA → CRA → Senior CRA → Lead CRA 
• Opportunity to become a GCC clinical research specialist (rare skillset in the market)

Work Environment:

• Fully remote between UAE monitoring visits (work from home in Saudi Arabia)
• Flexible hybrid model – plan your UAE trips efficiently around study needs
• International exposure working with French, Saudi, and Emirati medical teams
• Modern collaboration tools (Zoom, Microsoft Teams, cloud-based EDC/CTMS)
• Small, entrepreneurial team where your work directly impacts company growth
• Real responsibility and visible impact from day one

Compensation & Benefits:

• Competitive salary aligned with Saudi market standards for Junior CRA roles
• Premium health insurance coverage and GOSI
• Annual performance-based salary reviews
• Professional development budget for certifications and training

International Exposure:

• Work directly with French CRA experts (access to European best practices)
• Build your professional network across Saudi Arabia, UAE, France and Europe.
• Position yourself at the intersection of European excellence and GCC market growth
• Contribute to Vision 2030’s healthcare transformation goals

About Monitoring Force Gulf

Monitoring Force Gulf is a Franco-Saudi Clinical Research Organization with headquarters in Paris and operations in Riyadh / Jeddah. We specialize in helping international pharmaceutical, biotech, and medical device companies navigate SFDA regulatory pathways and conduct clinical trials in Saudi Arabia and the broader GCC market.

Our expertise bridges European regulatory standards with local Saudi and Gulf requirements, supporting Vision 2030’s healthcare transformation goals. We combine French clinical research excellence with deep knowledge of SFDA and GCC regulatory landscapes.