Early Development Associate Medical Director

What you’d do

Serves on cross-functional study execution teams for assigned trials, helping draft study protocols, investigator's brochures, and early development plans. Also prepares regulatory documents such as IND and CTA clinical sections and responses to regulators and ethics committees. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Clinical research experience
• Regulatory submission experience (IND/CTA)
• Strong oral and written communication skills
• Cross-functional team collaboration
• Global clinical research experience a plus