Clinical Research Physician (Principal Investigator/Sub-Investigator) - Full Time

What this role involves

This role involves conducting clinical trials as a principal or sub-investigator, ensuring participant safety and protocol compliance. Requires an MD or DO with at least 2 years as a licensed physician, and prior clinical research experience is preferred but not required. The position is onsite in Richfield, Minnesota, and does not offer visa sponsorship.

Skills this posting asks for

• ich gcp
• clinical research
• medical diagnosis
• treatment
• protocol compliance
• data integrity
• participant safety
• recruitment
• enrollment
• retention
• site initiation visits
• pre-selection visits
• investigator meetings
• medical oversight
• investigational medical product
• source management
• collaboration
• clinical operations
• regulatory
• pharmacy
• laboratory

Requirements

• 2 years of experience
• Level: mid
• Remote policy: onsite
• Visa sponsorship: no