Clinical Trial Associate I

Job Description

Qualifications

• •Bachelor's degree or equivalent in a clinical, biological, scientific, or health-related field
• •Knowledge of ICH / GCP and / or ISO14155 requirements and country-specific regulatory requirements
• •Proven ability to manage multiple projects in a fast-paced environment
• •Strong analytical and organizational skills

Benefits

Responsibilities

• •Assist in eTMF filing and administration, including document submission, review, and final collection
• •Support the study team with TMF functionality in accordance with study-specific plans and processes
• •Coordinate logistics for meetings, events, and training, and assist in disseminating related materials