Remote Executive Director, Medical Oncology

Summary

Join us today as an Executive Director, Medical to serve as a subject matter expert providing medical and scientific expertise and oversight to project teams and clients. The role involves leadership and mentorship to Senior Medical Directors and Medical Directors, supporting all aspects of Precision's business development activities, and serving as an internal source of medical and scientific guidance during client engagement.

Requirements

• MD, DO, MBBS, or equivalent medical qualifications
• A minimum of 10 years of experience in clinical research
• Line management experience or proven competencies for this position
• Experience in managing medical science aspects of complex and global trials
• Completed medical residency program
• Availability for domestic and international travel including overnight stays

Responsibilities

• Works with Senior leadership to support defined corporate and departmental medical strategies for Precision
• Directs, manages, and ensures collaboration within a team of Senior Medical Directors and Medical Directors in the planning, review, and analysis of medical activities on a global platform
• Serves as project physician
• Reviews and revises protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports, and new drug applications
• Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed
• Assists in the preparation of the Medical Monitoring Plan (if required) and materials for investigator meetings and staff training sessions
• Provides safety monitoring on assigned projects
• Interacts with other team members, study sites, and clients as needed
• Participates in feasibility discussions relating to specific project proposals
• Develops training modules and provides training in disease states across company
• Participates in training opportunities to advance medical knowledge keep up with drug development concepts
• Supports company's visibility and position with the CRO industry through publications and presentations
• Develops new and enhances existing client/investigator relationships whenever possible
• Participates in process improvement activities for company
• Other duties as assigned

Preferred Qualifications

• Phase I and Phase II oncology clinical trial experience
• Maintains current scientific and medical knowledge base
• Experience in managing complex and global trials
• CRO or biopharma industry experience preferred

Benefits

• Health insurance
• Retirement savings benefits
• Life insurance and disability benefits
• Parental leave
• Paid time off for sick leave and vacation