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Reading Time: 2 minutes Erika Singer, a member of the early talent acquisition team at Medidata, recently presented virtually to Rutgers University, University of California Berkeley, and Fordham University. Dozens of students from each university attended the info sessions and were eager to learn about Mediata and the potential opportunities we offer them both now and in the future. […]

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Reading Time: 4 minutesRuthie Davi, our VP of data science, and Jacob Aptekar, our senior director and trial design solutions lead, share their perspectives on the use of a Synthetic Control Arm, pioneered by Medidata Acorn AI, for more efficient trials in a regulatory setting. What is a Synthetic Control Arm? The randomized, controlled trial is well […]

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Reading Time: 2 minutesWe take pride in the Medidata way: Integrity. Honesty. Decency. Our fundamental values determine how we work and how we serve our customers. Trust is built and earned through years of commitment, accomplishment, and ethical behavior. At Medidata we’re proud of what we offer to the market because our technology and expertise consistently demonstrate these […]

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Reading Time: 2 minutes Early into the pandemic, some researchers were speculating about links between vitamin D deficiency and contracting COVID-19. Understanding the potential link for at-risk populations was the driving motivation behind this research, which was presented at the 2021 American Society of Clinical Oncology (ASCO) annual meeting. Vitamin D deficiency is easily detected and easily corrected. If […]

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Reading Time: 2 minutes While the COVID-19 pandemic certainly had an impact on enrollment for oncology clinical trials, you might be surprised at just how quickly enrollment began to improve, even as COVID-19 cases were on the rise. A group of researchers teamed up to study trends in oncology trial enrollment last year based on waves of the pandemic. […]

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Reading Time: 3 minutesOn April 19, the International Conference on Harmonization (ICH) made available an explanatory note and draft version of its updated principles for good clinical practice (GCP). While the principles are considered a “work-in-progress,” they offer an opportunity to reflect on the current vision of the working group and align with the modernized ICH E8 Revision […]

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Reading Time: 4 minutesThe Clinical Financial Blog was created to address the complexities that are encountered with financial management of clinical trials. With a lot of critical financial requirements still not fully understood and addressed, we’ve got you covered. Medidata’s team of experts, who have lived and breathed the budgeting and site payments processes, will provide first-hand experiences, […]

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Reading Time: 2 minutesWhen selecting an imaging technology solution, sponsors and CROs often focus on core capabilities like opening DICOM images, workflow management, and electronic case report forms. Query management allows communication between individuals performing quality assessments and management of the trial, and sites are often overlooked. Queries are important because they are commonly used to convey image […]

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Reading Time: 2 minutes With the availability of COVID-19 vaccines, the opportunity to work from offices in person has become more possible as the world slowly returns to normalcy. Internships have been an integral part of college students’ future careers, offering enormous benefits for both themselves and the organization they are involved in. But, as we entered 2021, many […]

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Reading Time: 2 minutes What was your favorite part about the internship experience? My favorite part about the internship experience was the time spent interacting with other interns. Since it was a fully virtual internship, we were not able to see each other in person so it was a bit difficult to get to know people. I had weekly […]

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Reading Time: 5 minutes This blog was authored by Fiona Maini, global compliance and strategy principal, Medidata. It goes without saying that the COVID-19 pandemic has had a tremendous impact on companies regardless of industry. The pandemic’s impact on clinical research globally has understandably been notable and has catalyzed greater adoption of remote strategies when conducting clinical trials. […]

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Reading Time: 2 minutesWritten in partnership with MIT Technology Review It’s easy to see the recruitment problem for investigators studying therapies for cancer and other deadly diseases: Patients with a life-threatening condition need help now. While they might be willing to take a risk on a new treatment, “the last thing they want is to be randomized to […]

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