Research Protocol Associate

Job Summary

A company is looking for a Research Protocol Associate to participate in clinical trial processes.

Key Responsibilities

• Assist with protocol and clinical research development, including regulatory documents and informed consent
• Coordinate study logistics, approvals, and protocol modifications
• Provide input to standard operating procedures and participate in assigned projects

Required Qualifications

• A bachelor's degree or an associate degree/certificate with 2 years of experience in clinical research or a related field
• Proficiency in Microsoft applications and familiarity with research systems
• Experience with regulatory documents and project management in clinical trials
• Ability to meet deadlines and work effectively in a remote environment
• Comfort with learning new data systems and contributing to process improvements