Remote Clinical Education Manager

Abbott Laboratories; Illinois; À distance; USD 99 000 - 199 000; Plein temps

Résumé du poste

Abbott is seeking a Manager of Clinical Education for its Vascular division. This is a fully remote role, leading teams within the Medical Affairs Sub-Function to implement policy and strategy and manage clinical trials and data collection.

The candidate will direct human clinical trials (Phase III/IV), recruit investigators, and ensure regulatory reporting, with a focus on compliance and high-complexity projects. Abbott emphasizes health benefits and career growth.

Qualifications

• Bachelor's degree in a field relevant to clinical research preferred.
• 5+ years of related experience; Master's with 3+ years acceptable.
• Experience as a CRA or direct clinical research in Medical Device/Diagnostics preferred.
• Knowledge of regulations affecting IVDs and Biologics.
• Has led several high complexity projects.
• ACRP or SoCRA certification preferred.

Responsabilités

• Oversee strategy implementation and operations for clinical trials and data collection.
• Contribute to protocol implementation and final reports.
• Recruit clinical investigators and negotiate study design/costs.
• Direct human clinical trials, Phases III/IV for products under development.
• Participate in adverse event reporting and safety monitoring.
• Coordinate reporting to regulatory agencies and ensure protocol adherence.
• Oversee investigator initiations and multi-site studies.
• May act as consultant/liaison with partner companies under licensing.
• Coordinate and provide reporting information for required submissions.

Formation

Bachelor's degree in clinical research or related field

Master's degree with 3+ years related experience

Description du poste

Abbott is seeking a Manager of Clinical Education for its Vascular division. This is a fully remote role, leading teams within the Medical Affairs Sub-Function to implement policy and strategy and manage clinical trials and data collection.

The candidate will direct human clinical trials (Phase III/IV), recruit investigators, and ensure regulatory reporting, with a focus on compliance and high-complexity projects. Abbott emphasizes health benefits and career growth.