Medical Director

About the role

In this role, you will serve as a key medical expert throughout the clinical trial lifecycle, partnering with project teams, investigators, and clients to support protocol execution, participant safety, and scientific excellence. In addition to medical monitoring responsibilities, you will contribute strategic medical insight to business development activities, proposal development, and study design, helping to shape innovative solutions for our clients.

What you'll do

• Primarily serve as the Global and/or Regional Medical Advisor on assigned clinical research projects
• Serves as Scientific Advisor and provides medical and scientific guidance to project teams, ensuring the highest standards of patient safety, protocol compliance
• Act as a trusted medical expert for investigative sites and study teams, supporting protocol interpretation, inclusion/exclusion determinations
• Review and provide medical input into study protocols, Investigational Brochures, Case Report Forms (CRFs), and other key study documentation
• Deliver therapeutic area and indication-specific training to clinical project teams

What you need

• 5–7 yrs of experience
• Clinical research
• CRO
• Documentation
• Pharmacovigilance
• Any graduate