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Clinical Research Coordinator

Clinical Research Coordinator

By: Blake
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Nurses, science grads, and healthcare admins entering research sites. Break-in + day-1 site ops (GCP, consent, source docs)—not pharma news or CRA travel shows. Audio for this show is produced with AI assistance. Episodes are researched, scripted, and reviewed for accuracy before release. Topics include: Clinical Research Coordinator.

Become a supporter of this podcast: https://www.spreaker.com/podcast/clinical-research-coordinator--7167796/support.© 2026 Let's Work This Sh*t Out
Episodes
  • Day-1 Break-In Site Ops: GCP Consent and Source Documents

    Day-1 Break-In Site Ops: GCP Consent and Source Documents
    Jul 11 2026
    In this episode, we break down the real first steps new coordinators need on day one and beyond—no fluff, just practical site ops. Learn how to ground your work in good clinical practice, master informed consent conversations, and keep source documents accurate from the start. These habits protect participants, satisfy monitors, and build confidence fast in a role where the first forty-eight hours set the tone.

    Key takeaways include:
    - Review core GCP principles the night before to follow protocols, report deviations same-day, and secure investigational products immediately.
    - Practice consent delivery by reading forms aloud, pausing for questions, and documenting exact times for signatures and discussions.
    - Record source data in real time—vitals, labs, adverse events—with precise dates, times, and details to avoid later gaps.

    A quick end-of-day cross-check keeps everything aligned and defensible. 📩 Have questions or want to share your experience? Reach out at .

    Support the show at https://www.spreaker.com/podca...

    📩 Have questions or want to share your experience? Reach out at prettyscumbag.nick@gmail.com.
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    4 mins
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