Medical Advisor

Responsibilities

• Oversee the direction, planning, execution, and data collection activities for clinical trials and research
• Contribute to the implementation of clinical protocols and facilitate the completion of final reports
• Recruit clinical investigators and negotiate study designs and costs
• Direct human clinical trials, specifically phases III and IV, for products under development
• Monitor adherence to protocols and determine study completion
• Participate in adverse event reporting and safety monitoring responsibilities
• Coordinate and provide reporting information for submissions to regulatory agencies
• Act as a consultant or liaison with other corporations under licensing agreements

Requirements

• Associates Degree
• Minimum 1 year of experience in a relevant field
• Experience with clinical trial oversight and data collection
• Proficiency in protocol implementation

About the Company

Abbott is a global healthcare leader dedicated to the power of health. For more than 135 years, we have been helping people reach their potential through innovative solutions in diagnostics, medical devices, science-based nutrition, and branded generic medicines. With a presence in more than 160 countries, we work to advance life-changing technologies that help people live their best lives.