Clinical Study Specialist

Job Summary

A company is looking for a Clinical Study Specialist, Sponsor Dedicated.

Key Responsibilities

• Assist in the planning, initiation, and execution of clinical trial activities
• Conduct site feasibility assessments and participate in site selection processes
• Coordinate with investigative sites to ensure compliance with study protocols and regulatory requirements

Required Qualifications

• Bachelor's degree in a relevant field, such as life sciences or healthcare
• Previous experience in clinical research or a related field preferred
• Strong organizational skills
• Ability to work independently and collaboratively in a fast-paced environment
• Ability to prioritize tasks effectively