Job Summary

A medical device company is in need of a Telecommute Post Approval Clinical Surveillance Principal Clinical Research Specialist.

Core Responsibilities of this position include:

• Conducting registered and non-registered clinical studies
• Overseeing and interpreting results of clinical investigations
• Overseeing and resolving operational aspects of clinical trials

Qualifications Include:

• Bachelor's degree AND
• 7 years of clinical research experience OR
• Advanced degree AND
• 5 years of clinical research experience
• Ability to oversee, design, plan and develop clinical evaluation research studies
• Prepares and authors protocols and case report forms