If AI can write the first draft of a clinical study report in less than a day, why pay a medical writer? This is a scary consideration and can leave writers feeling defensive. But medical writers’ true adversary is refusal to embrace this technology and make it work for us.
Those who do not work directly in TMF, or document management, often feel little obligation as a TMF stakeholder, or do not recognize they are a stakeholder. They may have undergone general TMF training, and they still do not quite understand their departmental role within the TMF.
Learn how a site-centric partnership can thrive when all parties involved, including study monitors/regional site managers, principal investigators, patients, and study coordinators, understand the potential challenges and unique needs of each trial and can face them together.
In part two of this webinar series, presenters focus on avoiding potential risks such as unexpected budget changes and unplanned change orders that could jeopardize the success of a clinical trial. Watch now to explore common red flags, ask critical questions, and adopt best practices to safeguard your trial's budget.
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