Country Study Lead — Global Clinical Trial Manager

KCR Placement; Bell (CA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning offerings

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions is seeking a Country Study Lead/Clinical Trial Manager to oversee day-to-day clinical trial management activities and deliver high-quality outcomes across our programmes. You will lead cross-functional teams, establish trial protocols, and manage relationships with investigators while ensuring compliance with global regulations.

The role requires solid trial management experience, the ability to handle competing priorities, and a willingness to travel about 25%.

Qualifications

• Solid clinical trial management experience and ability to manage competing priorities.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is preferred.

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring adherence to 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 local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Team leadership

Education

University degree in medicine, science, or equivalent combination of education & experience

Job description

ICON Strategic Solutions is seeking a Country Study Lead/Clinical Trial Manager to oversee day-to-day clinical trial management activities and deliver high-quality outcomes across our programmes. You will lead cross-functional teams, establish trial protocols, and manage relationships with investigators while ensuring compliance with global regulations.

The role requires solid trial management experience, the ability to handle competing priorities, and a willingness to travel about 25%.