Clinical Research Coordinator

Support AI training initiatives with clinical research expertise, protocol review, and structured data collection for healthcare AI tools.

Role details

• Domain: Healthcare
• Experience level: Masters+
• Required expertise: Clinical Trials, GCP Compliance, Data Collection, IRB Protocols
• Location: Fully remote

Responsibilities

• Review and annotate clinical trial documentation
• Validate AI-generated research protocol summaries
• Assist in structuring medical datasets for AI training
• Flag inconsistencies in clinical content

Requirements

• Masters degree in clinical research, public health, or related field
• 2+ years experience coordinating clinical studies
• Working knowledge of GCP and IRB processes
• Detail-oriented with strong data skills

Benefits

• Fully remote with flexible hours
• Contribute to meaningful healthcare AI
• Work with top research professionals

Pasiflora AI is an expert network that contracts specialists to review, annotate and validate AI training data in their own field. Screening steps, task volume, time commitment and payment terms are shown on the Pasiflora application page — apply on pasifloraai.com.