Clinical Trial Manager — Global Study Lead

Abbott; Madison (WI); On-site; USD 78,000 - 156,000; Full time

Job summary

Abbott is seeking a Clinical Trial Manager to lead and support the management of clinical studies in a fast-paced environment. You will oversee day-to-day study operations, ensure timelines and budgets are met, and collaborate with investigators, vendors, and internal teams in Madison, WI or San Diego, CA.

The role requires 5+ years in clinical research, strong project leadership, and familiarity with GCP/ICH quality standards. Travel up to 20% may be required.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 5+ years of experience in clinical research.
• 1+ year of experience leading project teams through start-up, conduct, data management, analysis, close-out and reporting.

Responsibilities

• Coordinate operational aspects of studies including planning, start-up, enrollment and close-out.
• Prepare study plans, timelines, protocols, consent forms, recruitment and monitoring plans, budgets and site contracts.

Skills

Clinical Research

Project Leadership

Monitoring

Protocol Writing

Quality Standards

US Work Authorization

Vendor Oversight

Education

Bachelor's degree in life sciences

Job description

Abbott is seeking a Clinical Trial Manager to lead and support the management of clinical studies in a fast-paced environment. You will oversee day-to-day study operations, ensure timelines and budgets are met, and collaborate with investigators, vendors, and internal teams in Madison, WI or San Diego, CA.

The role requires 5+ years in clinical research, strong project leadership, and familiarity with GCP/ICH quality standards. Travel up to 20% may be required.