One of the most special things about Pharmaceutical Executive®, in my opinion, is when people share their stories—where they came from; how their upbringing or education or background impacted their desire to work in pharma; any personal ties to their work, such as finding new treatments in a specific disease state due to a loved one having been impacted by that same disease; and just generally sharing their passion for their work. As someone who’s worked in pharma journalism for many years, there’s something extraordinary to hear about the why for individuals.
That isn’t any less true for Lisa LeCointe-Cephas, SVP, chief ethics and compliance officer and office of general counsel, human health, Merck. In this issue, our executive profile, written by Lisa Henderson, features LeCointe-Cephas. Prior to working in pharma, LeCointe-Cephas set out to be a doctor and pivoted to become a lawyer due to her interest in people and what makes them tick. She worked in securities litigation and white-collar criminal defense, specifically for Kirkland & Ellis LLP. As you can imagine, her experiences there impacted how she approaches leadership in her work at Merck, specifically about how to communicate effectively. She also emphasized the importance of not focusing on negative thoughts when you “fail” and make mistakes but instead focusing on how to do things better next time. She also adopted a stop-drop-roll mantra, which I found really interesting and unique. But I won’t spoil that one for you.
Also in this month’s issue is our annual Product Launch coverage. We feature five drugs that our editorial board and team thought were especially impactful in the industry and to the lives of patients:
Thank you to everyone who contributed insights, articles, and time to this issue. Without you all, we couldn’t do what we do!
To Tackle the Plastic Waste Crisis in Pharma, Here’s Where to Start
October 30th 2024By demonstrating big advancements in recycling, pharma companies will be much more likely to attract shareholders and other investors, giving themselves a leg up in the competition to lead the biopharmaceutical industry well into the future.
Solving One of the Hardest Questions in Cancer: How Do We Ensure Patient Access to Medicines?
October 16th 2024Pharmaceutical companies are facing new guidelines, laws, and regulations requiring a reconsideration of how to prioritize, develop, commercialize, and ultimately, secure access to medicines.
Leverage AI to Lower Cost, Barriers to Cell Therapies
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