Global Study Director - Senior Clinical Project Leader

ICON; Burlington; On-site; CAD 90,000 - 110,000; Full time

Job summary

A global healthcare intelligence company is seeking a Global Study Associate Director in Burlington, Newfoundland and Labrador. The successful candidate will lead cross-functional teams to manage clinical studies, ensuring timelines, budget, and quality standards are met. With at least 7 years of clinical experience and oncology knowledge, this leadership role offers a competitive salary and a range of benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• At least 7 years of relevant clinical experience in the pharmaceutical industry.
• 2 years of project management experience, global level is desirable.
• Deep understanding of clinical operations and study management processes.
• Oncology/hematology experience required.

Responsibilities

• Lead cross-functional study team to ensure clinical study progress.
• Ensure compliance with governance controls.
• Oversee Trial Master File completion.
• Develop and maintain relevant study plans.

Skills

Clinical operations understanding

Cross-functional team leadership

Conflict management

Critical thinking

Decision-making

Effective communication

Education

University degree in medical or biological sciences

Advanced degree preferred

Job description

A global healthcare intelligence company is seeking a Global Study Associate Director in Burlington, Newfoundland and Labrador. The successful candidate will lead cross-functional teams to manage clinical studies, ensuring timelines, budget, and quality standards are met. With at least 7 years of clinical experience and oncology knowledge, this leadership role offers a competitive salary and a range of benefits focused on well-being and work-life balance.