Medical Monitor

Overview

Role involves providing clinical support and medical advice throughout clinical trials.

Ideal candidate should have at least 2 years of medical experience and knowledge of clinical trials.

Locations

• Canada, Quebec
• United States, Pennsylvania

Requirements

• Degree in medical disciplines
• At least 2 years of medical experience
• Knowledge of clinical trial process

Responsibilities

• Provide clinical support throughout clinical trial lifecycle
• Answer medical questions
• Review study data
• Analyze study data/results
• Write and review protocols and reports
• Provide training in disease/therapeutic area
• Assist in investigator site selection
• Participate in subject recruitment activities