As a Director of Consulting Services at CGI, Meghan Miller is dedicated to helping clients become high-performing, digitally connected and compliant. Focused on the pharmaceutical industry, she works with clients to identify problems and offer innovative solutions, which enable them to create a healthier world.
Archives: Speakers
Dana Baki
Dana Baki is the Chief Commercial Officer of The Exploration Company, one of the fastest growing space companies globally, building reusable space capsules and lunar landers. This Nyx capsule will be the first to use green propellant globally, while flying at a fraction of the cost of global competition.
Prior to joining The Exploration Company, Dana was the co-founder & COO of MUNCH:ON, a food technology platform based out of the Middle East, that was acquired by Careem (Uber’s subsidiary in the region). Before starting MUNCH:ON, Dana was a Partner of Business Development at AlJal Capital—a financing and venture capital firm in the United Arab Emirates. Previous to that, Ms. Baki worked for Procter & Gamble in the United States for 7+ years, benefiting from a wide range of assignments within the company and gaining expertise in Corporate Strategy, Marketing and Consumer Insights.
She holds an MBA from Georgetown University and B.A. in Economics and English Literature from The University of Michigan.
Giulia Ferrati
Giulia Ferrati is a sustainability professional, experienced in leading the development, implementation and governance of the Corporate Responsibility and Sustainability strategy for global and fast paced enterprises across different industries
Chris Engel
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Chris Engel possesses a strong background in logistics and has gained intercultural work experience in China and Switzerland. Since 2008, he has held several sales responsibilities and roles in logistics, handling major worldwide accounts at TNT Express and FedEx. Chris joined World Courier in 2014, bringing this invaluable experience in managing global pharmaceutical clients to the organization as a Global Account Manager. During his tenure, he has been involved in and led numerous projects involving high-value specialty drugs and shipments of exceptional sensitivity, with low tolerance for temperature deviations and challenging time requirements. He has utilized his expertise to manage and design complex supply chains for both global clinical trials and commercial drugs. Joining the Services team in July 2019 and subsequently rising to the position of Commercial Supply Chain (CSC) Director in May 2020, Chris has been a driving force behind crucial initiatives for CSC’s expansion. He assists clients in transitioning from clinical to commercial drug logistics, encompassing product launches, drugs with volatile demand, and a wide range of volumes from single dosages to bulk shipments. As of 2023, he has been elevated to the role of Services Development Director, wherein he drives the process of introducing innovative services to the market, closely aligned with customer needs and market trends. |
Katelynn Spingola
Katelynn Spingola brings nearly a decade of invaluable experience in healthcare and research to her role as Associate Director of Clinical Site Operations at EmVenio Research. Leading teams across multiple locations in the East and Central time zones, Katelynn is dedicated to making a tangible impact within their respective communities. Under her adept guidance, these teams function as vital advocates, diligently working to raise awareness, educate the public, and establish a strong local presence. Katelynn’s primary objective is optimizing site operations to ensure each location meets enrollment goals across a diverse array of study indications. Her extensive expertise in clinical research ensures that these endeavors lead to successful outcomes and good clinical data. Katelynn’s leadership style is marked by a commitment to community engagement and operational excellence, positioning her as a pivotal figure in advancing the mission of EmVenio Research.
Rachael Sawaya
Rachael Sawaya is an Associate Director of Project Management at PCM Trials with over seven years of experience in the clinical research field. Prior to PCM Trials, she worked as a clinical research coordinator where she gained extensive knowledge of working at the site and has taken that experience to reduce the burden and better support sites to implement mobile visits. At PCM Trials, Rachael oversees the execution of mobile visits across a wide variety of therapeutic areas and on a global scale. She supports clients throughout the implementation of mobile visits to maintain customer satisfaction and implement efficiencies across therapeutic areas and geographies. Rachael is passionate about implementing solutions for participants that increase participant engagement to ensure clinical trials can obtain critical long-term data, especially in rare disease and vulnerable patient populations.
Betty McGregor
Betty has 20+ years of clinical research experience in various roles at the site and CRO, and has been with ICON for over 5 years now. Her experience traverses varying therapeutic areas and phases, but falls mostly in oncology/hematology early phase trials.
Dr. Sara Doan
Dr. Sara Doan is the Executive Director, Program Strategy and Delivery for Internal Medicine & Neuroscience at TFS HealthScience. She brings a robust 27-year background in global clinical research to her role, with a particular emphasis on psychiatry over the past 12 years. Her expertise spans a broad range of disorders including Alzheimer’s, Parkinson’s, Narcissistic Personality Disorder, Borderline Personality Disorder, Major Depressive Disorder, Post Traumatic Stress Disorder, Bipolar Disorder, Migraine, and Anxiety. Dr. Doan is a Doctor of Chiropractic with a specialization in the Central Nervous System, having earned her degree from Parker University in Dallas, Texas. She is proficient in both English and Farsi.
Marissa M. Ballesteros
Marissa M. Ballesteros, RN, MPH, MBA, serves as the Senior Director of Clinical Data & Sensor Strategy at Medidata, where she specializes in commercial strategy development and establishing partnerships with sensor technology companies. With a career spanning over two decades, Marissa has honed her expertise in leading clinical trial operations, having held pivotal roles at industry giants such as Pfizer, Roche, Scripps Translational Science Institute and Qualcomm. Marissa’s professional background uniquely blends clinical acumen gained from her experience as a wellness and cardiology nurse with a keen business insight cultivated through involvement in diverse areas such as due diligence for in-licensing and mergers & acquisitions, key opinion leader (KOL) management, budgeting/contracting, and pharmaceutical sales.
Kelsey Buhler
Kelsey Buhler has been a Product Specialist at Viedoc Technologies since 2021, and specializes in providing technical demos, support, and project management for Viedoc study builds. Prior to her role at Viedoc, she has 7 years combined experience as a Data Manager/Project Manager at a Medical Device CRO, a Data Entry Specialist, and a Clinical Subjects Associate, where she would obtain consent from subjects in clinical trials. All these experiences drive her passion for user-friendly Electronic Data Capture (EDC) systems that increase efficiencies for the subjects, site, and all other study users.