Clinical Trial Specialist

Job Description

Qualifications

• •Bachelor's degree in life sciences, clinical research, or a related field
• •Extensive experience in site management, clinical operations, or monitoring within the clinical research industry
• •Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements
• •Ability to manage multiple sites and timelines effectively
• •Experience in preparing and maintaining site management documentation

Benefits

Responsibilities

• •Oversee day-to-day site management activities ensuring compliance with study protocols and regulatory requirements
• •Collaborate with site staff and cross-functional teams to resolve issues and ensure timely data collection
• •Assist with site initiation, monitoring visits, and close-out activities while providing guidance to junior staff