Clinical Trials Specialist

Job Summary

A company is looking for a Clinical Trials Specialist to manage protocol teams in clinical trials related to HIV and other infectious diseases.

Key Responsibilities

• Leads protocol development, study start-up, and study conduct activities
• Develops and manages study-specific ancillary documents and communicates study progress
• Partners with cross-functional teams and resolves issues encountered during all study phases

Required Qualifications

• Master's degree in public health, social sciences, or related discipline preferred, with two years of relevant experience
• Bachelor's degree may be accepted with five years of relevant experience
• Experience leading protocol development and writing clinical research protocols is required
• Experience with HIV, hepatitis, and/or tuberculosis trials is preferred
• Strong organizational skills and ability to manage multiple tasks simultaneously