Clinical Research Manager MSD

Key Responsibilities

• Serve as the main point of contact for assigned protocols, representing country operations within global Clinical Trial Teams

• Lead end to end project management of clinical trials from feasibility and site selection through execution and close out

• Ensure compliance with ICH/GCP, local regulations, internal policies, and safety reporting requirements

• Drive study performance by proactively planning, tracking, and resolving risks related to timelines, quality, and recruitment

• Lead and coordinate local study teams, acting as protocol expert and supporting CRAs and other country roles

• Review monitoring visit reports, identify performance gaps, and escalate issues as needed

• Conduct quality control visits when required

• Develop and execute local risk management plans for assigned studies

• Ensure accurate and timely use of CTMS, eTMF, and other key systems

• Build strong, trust based relationships with investigators, vendors, and external partners

• Share best practices across studies, countries, and clusters

• Contribute to local and regional clinical operations strategy in collaboration with internal stakeholders

Core Skills

• Strong project and site management expertise

• Solid understanding of clinical trial planning, execution, and performance metrics

• Excellent knowledge of the local regulatory environment

• Ability to manage multiple studies and priorities simultaneously

• Fluent in English and local language (Arabic), with strong written and verbal communication skills

Leadership & Behaviors

• Proven ability to lead without direct authority and influence cross functional teams

• Strong problem solving and risk mitigation mindset

• Skilled in navigating complex situations such as recruitment challenges, compliance issues, and resource constraints

• Collaborative, culturally aware, and effective in remote/virtual environments

• Professional, diplomatic, and confident when engaging with investigators and stakeholders