Executive Medical Director Oncology

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe. Won’t you join us today as an Executive Medical Director?

Position Summary: 

The Executive Medical Director serves as a subject matter expert providing medical and scientific expertise and oversight to project teams and clients.  Provides leadership and mentorship to Senior Medical Directors and Medical Directors.  Provides support that encompasses all tasks from project concept and development through study execution to the final study report and/or submission.  The Executive Medical Director supports all appropriate aspects of Precision’s business development activities and serves as an internal source of medical and scientific guidance during client engagement. 

Essential functions of the job include but are not limited to:  

• 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 

Qualifications: 
Minimum Required: 

• MD, DO, MBBS, or equivalent medical qualifications  
• A minimum of 10 years of experience in clinical research 
• Line management …