Clinical Research Manager – IROS
National Reference Laboratory
Date: 2 weeks ago
                            City: Abu Dhabi
                                                        Contract type: Full time
                                                    
                                                
                            ID
      
      
       2025-4834
      
     
     
      
       Category
      
      
       Clinical Operations
      
     
     
      
       Asset : Name
      
      
       IROS (Insights Research Organization & Solutions)
      
     
     
      
       City
      
      
       Abu Dhabi
      
     
    
   
  
 
 
We are seeking a Clinical Research Manager to join IROS, the UAE’s first homegrown Contract Research Organization (CRO), dedicated to raising the bar in clinical trial management and research excellence
                    Overview
M42’s Integrated Health Solutions (IHS) platform drives transformative national programs and population health initiatives, addressing global health challenges through precision, prevention, and predictive care. Flagship initiatives include the Emirati Genome Program (EGP), the Abu Dhabi BioBank, and Biogenix Labs, which together advance personalized medicine, drug discovery, and biobanking excellence. Environmental Sciences complements these efforts by analyzing non-human factors impacting health, while IROS (Integrated Research Organization Solutions) powers clinical innovation through high-quality researchWe are seeking a Clinical Research Manager to join IROS, the UAE’s first homegrown Contract Research Organization (CRO), dedicated to raising the bar in clinical trial management and research excellence
Responsibilities
- Lead, mentor, and manage a team of Clinical Research Associates (CRAs).
 - Oversee clinical trial execution with adherence to GCP, regulations, and SOPs.
 - Collaborate with Clinical Project Managers to align on deliverables and resources.
 - Conduct on-site performance evaluations and manage staff development plans.
 - Drive process improvements and ensure consistent compliance across studies.
 - Handle administrative oversight, including approvals, performance reviews, and onboarding.
 
Qualifications
- Bachelor’s degree in Life Sciences (or equivalent).
 - 5+ years’ experience as a CRA/Monitor and at least 4 years in a lead/project role.
 - Proven ability to lead teams within global/multi-regional clinical trials.
 - Strong knowledge of clinical research processes, ICH/GCP guidelines, and regulatory requirements.
 - Excellent communication, organizational, and leadership skills.
 - Experience with electronic data capture (EDC) and budget management preferred.
 
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