Clinical Trials Lead: Strategy, Operations & Delivery

Abbott (abbottcareers2 board); Madison (WI); On-site; USD 120,000 - 170,000; Full time

Job summary

Abbott is seeking a Clinical Trial Manager to lead and support the management, planning, execution, and closure of clinical studies in a fast-paced environment. The role may be based in Madison, WI or San Diego, CA, requiring travel up to 20%.

You will work across study planning, budgets, site selection, data handling, and vendor management to ensure timely, compliant execution of clinical research plans.

Qualifications

• Bachelor's degree in the life sciences or field as outlined in the essential duties.
• Minimum 5 years of clinical trial management experience.

Responsibilities

• Coordinate and oversee the operational aspects of a study including planning, start-up, enrollment and close out activities.
• Prepare, review and implement study related plans and documents including project timelines, study protocols, informed consent forms, recruitment plans, monitoring plans, study budgets, site contracts & budgets, vendor management plans.
• Develop plans for systems and materials required to support the efficient execution of clinical studies and manage during the conduct of the study.
• Develop, implement and maintain tools to manage, monitor and report on study health & operations, timelines, and study finances to management and stakeholders.
• Oversee sample management activities including planning, sample handling, kit supply management, sample shipping, processing, and results.
• Develop site recruitment plans and identify, select, start-up and monitor clinical research sites.
• Oversee study budgets and budget management including site contracting and budget negotiations, invoice review and accrual management.

Skills

5+ years experience

Education

Bachelor's degree in life sciences

Job description

Abbott is seeking a Clinical Trial Manager to lead and support the management, planning, execution, and closure of clinical studies in a fast-paced environment. The role may be based in Madison, WI or San Diego, CA, requiring travel up to 20%.

You will work across study planning, budgets, site selection, data handling, and vendor management to ensure timely, compliant execution of clinical research plans.