Research Protocol Associate

Job Summary

A company is looking for a Research Protocol Associate to support clinical trial development and maintenance.

Key Responsibilities

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

Required Qualifications

• Bachelor's degree or associate degree 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 of clinical trials
• Ability to meet deadlines and work effectively in a remote environment
• Desire for teamwork and excellence in supporting clinical study operations