Clinical Trial Researcher

Job Summary

A company is looking for a Clinical Trial Researcher responsible for administrative support related to clinical studies.

Key Responsibilities

• Provide comprehensive administrative support for clinical trial operations and maintain study documentation
• Manage documentation processes to ensure compliance with regulatory and GCP standards
• Assist in the preparation and submission of IRB documents and monitor adherence to study protocols

Required Qualifications

• Bachelor's degree or equivalent combination of experience, education, and training
• 2+ years of experience at the Sponsor or CRO level, or 5 years at the SMO or site level
• Experience with medical device clinical studies preferred
• Familiarity with clinical development standards and regulatory requirements (GCP, FDA)
• Experience with shoulder arthroplasty or orthopedics is a benefit but not essential