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Clinical Research Manager – IROS at Mubadala Health
, , -
Full Time

Start Date

Immediate

Expiry Date

11 Jan, 26

Salary

0.0

Posted On

13 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Team Leadership, GCP Compliance, Project Management, Performance Evaluation, Process Improvement, Staff Development, Communication Skills, Organizational Skills, Regulatory Knowledge, Electronic Data Capture, Budget Management

Industry

Hospitals and Health Care

Description
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 research. 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. 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.
Responsibilities
Lead and manage a team of Clinical Research Associates while overseeing clinical trial execution. Ensure adherence to GCP, regulations, and SOPs, and drive process improvements across studies.