Take ownership of clinical study monitoring * You stay closely connected with your study sites, ensuring continuous support and follow-up * Most importantly, you safeguard the rights, safety, and well-being of study participants * You assist with contracts, invoices, and other study related financial aspects * You create a positive, collaborative study environment * You've gained 2–3+ years of experience in clinical research, including working as a CRA — ideally within medical device studies * You're open to travel (typically 30–70%) and enjoy being close to your study sites * You work independently, stay organized, and can manage multiple sites or studies at once
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