Clinical Research Assistant

📋 Description

• Project support inclusive of project planning, preparation of paperwork and documentation, and
• Data collection
• Audits (both virtual and in person)
• General preparation and closing of studies
• Working with IRB submissions
• Assisting with Study participant recruitment inclusive of phone and in person screening and subject

🎯 Requirements

• Certified CRA credential ideal
• Minimum 1+ years experience in clinical research
• Experience in regulatory aspects of Phase I-III clinical IND trials and experience with FDA audits
• Experience with Microsoft platforms, EMR and EHR (electronic health record) systems and CTMS
• Experience with phlebotomy preferred
• Authorization to work in the United States indefinitely without restriction or sponsorship

🎁 Benefits

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays