Clinical Project Lead

M42 Health; Abu Dhabi; On-site; AED 200,000 - 300,000; Full time

Job summary

A leading company in the UAE's healthcare sector is hiring a Clinical Project Lead to oversee clinical trials. The chosen candidate will manage study execution, regulatory submissions, and collaborate with internal and external stakeholders while ensuring compliance with ICH-GCP and company SOPs. This role requires strong leadership and extensive experience in clinical research, making it a pivotal position within the organization.

Qualifications

• Minimum 6 years of clinical research experience with 5+ interventional clinical trials.
• Experience with Phases I-IV trials preferred.
• Strong knowledge of ICH-GCP, FDA, and CTA processes.

Responsibilities

• Serve as primary liaison between sponsors, sites, and internal teams.
• Manage regulatory submissions and compliance.
• Supervise team members and support business development.

Skills

Leadership

Communication

Organization

Analytical skills

Education

Bachelor's degree in Life Sciences

Tools

MS Office

Job description

Bachelor of Business Administration(Management)

Nationality

Any Nationality

Vacancy

1 Vacancy

Job Description

Job Description

Overview

IROS is the first UAE-based Contract Research Organization (CRO), specializing in healthcare research and committed to the highest scientific and ethical standards. A proud member of the M42 network, Abu Dhabi s leading HealthTech ecosystem backed by Mubadala and G42, IROS delivers clinical trial management and real-world data integration services across all therapeutic areas.

As a Clinical Project Lead, you will oversee the full lifecycle of clinical trials, ensuring timely, high-quality delivery while serving as the main point of contact for sponsors, sites, and internal stakeholders. The role involves managing all aspects of study execution including regulatory submissions, site operations, vendor management and project milestones, while driving collaboration across all stakeholders.

Responsibilities

• Serve as primary liaison between Sponsor, sites, and internal teams.
• Manage EC/RA submissions and compliance with regulatory timelines.
• Oversee study milestones, progress tracking, and reporting.
• Conduct co-monitoring visits with CRAs, support CRA performance and ensure monitoring report quality.
• Coordinate with internal/external stakeholders and third-party vendors.
• Lead the development, review and approval of essential project documents.
• Manage Investigator Meetings, contracts, and logistics.
• Supervise team members, provide feedback, and support business development.
• Ensure adherence to ICH-GCP and company SOPs.
• Serve as Project Manager for smaller-scale trials.
  
  

Qualifications

• Bachelor s degree in Life Sciences or equivalent.
• Minimum 6 years of clinical research experience; including 5+ interventional CTs.
• Experience with Phases I-IV trials and prior CRO/sponsor background preferred.
• Advanced knowledge of ICH-GCP, FDA, and CTA processes.
• Strong leadership, communication, organizational, and analytical skills.
• Proficiency in English and MS Office; valid driver s license.
• Ability to manage multiple tasks and work under pressure.
  

Company Industry

• Medical
• Medical Devices

Department / Functional Area

• Administration

Keywords

• Clinical Project Lead

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