Most CROs ask for onsite monitoring experience for CRA roles. As CTAs, we already support many CRA activities and understand study operations closely, yet getting that first onsite opportunity remains difficult.

Requesting organizations and experienced CRAs to support aspiring professionals through shadow visits, co-monitoring, and transition opportunities.

Fellow Clinical Research professionals and CRAs — would love to hear your thoughts and experiences.

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Hey everyone,

I hope you’re doing well!

Based on my experience as Clinical Research Assistant at Sleepiz (Site Monitoring) - Six Sigma Master Black belt - GCP certified by ISCR - Certified Marketer - Trainee at MITCON Bio Pharma Center - Medical Biotechnologist - Biotechnologist.

I've been searching roles in Clinical monitoring and related opportunities especially in Medical Devices Regulatory Affairs.

Please help😊

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