Clinical Trial Manager: Lead Global Trials & Compliance

ICON Strategic Solutions; Malaysia; On-site; MYR 150,000 - 240,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Malaysia is seeking a Clinical Trial Manager to oversee day-to-day clinical trial operations. You will support your team to deliver high-quality outcomes across our programmes, ensuring adherence to timelines, budgets, and quality standards.

Responsibilities include collaborating with cross-functional teams, building relationships with investigators, and ensuring compliance with local, national, and international regulations. Travel of ~25% is required as needed.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is preferred.
• Willingness to travel as required (approximately 25%).

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Regulatory compliance

Vendor management

Stakeholder management

Travel willingness

Education

University degree in medicine, science, or equivalent

Job description

ICON Strategic Solutions in Malaysia is seeking a Clinical Trial Manager to oversee day-to-day clinical trial operations. You will support your team to deliver high-quality outcomes across our programmes, ensuring adherence to timelines, budgets, and quality standards.

Responsibilities include collaborating with cross-functional teams, building relationships with investigators, and ensuring compliance with local, national, and international regulations. Travel of ~25% is required as needed.