Jackie comes to us with over 30 years of experience in IT and Clinical Development. In 2001, Jackie accepted a role in Clinical Development and that is where she continued building her leadership career.

Prior to Medidata, Brian was in the CRO space for 15 years where he supported RBQM for the past 8 years specializing in RBQM operationalization for small to large pharma, biopharma, and biotech companies specializing in implementation of ICH E6 (R2).

Michael is a member of Medidata’s Mobile Health team and is a subject matter expert in electronic informed consent and virtual trials.  Over the last six years, Michael has worked collaboratively with sponsors, CROs, regulators, ethics committees and researchers around the world to pioneer the use of electronic informed consent and virtual trials.

Wayne is Senior Vice President, Rave Platform Technology at Medidata. Wayne oversees the strategy, development, and delivery of Rave EDC, Rave RTSM, Rave Coder and Rave Safety Gateway across all R&D disciplines.

Prior to joining Medidata, Wayne spent 12 years overseeing Product Management for clinical technology used by Data Management and Biometrics at PRA Health Sciences.

Kelly McKee is the Vice President of Patient Registries and Recruitment at Medidata with 20 years of experience in clinical trial operations, patient recruitment and innovation.

She is a proven clinical trial leader and trailblazer in operationalizing global patient-focused solutions across organizations including innovations in clinical trial awareness, access, and improvements in patient experiences.

Kelly is passionate about celebrating the role that clinical trial participants bring in making new medicines and vaccines possible and was named one of PharmaVoice’s 100 Most Inspiring Leaders in 2020, Centerwatch’s Top 20 Innovators of 2018, and PharmaTimes’ Clinical Researcher of the Year, Clinical Research Teams, in 2012.

Ben McConnochie is responsible for Medidata’s new clinical trial & Real World Data linkage solution, Medidata Link.

Jonathan is responsible for helping Medidata clients adopt innovative solutions to drive digital transformation across sponsor, site and patient workflows. He has over 30 years of experience building, implementing and managing clinical trial technology over his career at Oracle Health Sciences, IBM, Parexel and IQVIA. He has worked extensively across global projects within eClinical, clinical analytics, decentralized trials and sensors.

A Stanford Medicine X e-Patient scholar, Marie Ennis O’Connor brings a wealth of experience to the co-creation of person-centered outcomes within clinical and innovation spaces. With a focus on moving beyond the rhetoric of patient involvement towards operational implementation, her work brings key stakeholders together to engage in meaningful ways. In 2020, she received a HIMSS Future 50 award. The Health Information and Management Systems Society (HIMSS) awards recognize health leaders who have made significant contributions to digital health worldwide. Awardees work with HIMSS and the global healthcare community to overcome systemic health challenges by addressing gaps at the local and regional level.

Mark guides RTSM solution design and integration in support of the pharmaceutical and medical device sectors. He brings over 20 years of experience in startup, systems integration and project management roles with PwC and IBM Global Consulting Services. In his current role, Mark collaborates with an interdisciplinary team of biostatisticians, clinical supplies and operations specialists, product engineers and project managers to envision and develop effective IRT solutions.

Sarah Westall is a Solutions Sales Specialist in Connected Data responsible for the business development of growing one of the world’s most sophisticated networks dedicated to providing secure, powerful and intelligent management and workflows of medical images for the life sciences industry.

Paul O’Donohoe is Scientific Lead, eCOA and Mobile Health at Medidata Solutions, a clinical software platform provider.

Meghan is responsible for driving the strategic direction of the Grants Manager and Payments products. An accomplished hands-on leader with over 15 years in the life science technology industry, Meghan has significant experience in the investigator grant administration domain having led and provided oversight to the successful technology adoption efforts for clients ranging from Top 10 CROs to small and mid-size Sponsor companies.

Clare has over 25 years experience within clinical research over diverse functions and phases. She started her career in Internal Regulatory Affairs and then moved into Data Management before taking further opportunities at Covance within the Phase I Clinical Research Unit where she managed the clinical staff including project management, clinical data monitoring and volunteer recruitment. Clare then decided to concentrate her career within Project Management and moved to the position Executive Director, Global Project Delivery at Labcorp. 

Aman is a physician, digital health futurist, and pharmaceutical executive focused on developing revolutionary technologies to increase healthcare accessibility, predict disease onset, prevent diseases and progression, and improve health outcomes worldwide. He is currently the SVP of Global BioPharma at AliveCor, where he oversees global strategic partnerships with CROs and pharmaceutical companies. Aman has over a decade of experience as a worldwide medical leader at leading pharmaceutical companies including Novartis, GSK, and Sanofi.

Rachel is the Product Lead for our newly launched Trial Impact Analytics offering.

At Medidata, Alicia works to infuse the patient perspective throughout the product development lifecycle and help engage patients in novel ways.

22 years of global Clinical Research experience in project delivery (as CRA, Clinical Lead and Project Manager) in Pharma and CROs.

Trishna Bharadia, BA(hons), MFPM( Hon) is a multi-award winning health advocate and patient engagement champion.

Tanmay is a Senior Director at Medidata Medidata AI. He has 10+ years of experience advising Biopharmas and Biotechs on data and analytics across R&D, medical affairs, and commercial functions. He is passionate about getting life-saving and innovative medicines to patients faster by running more efficient clinical trials. At Medidata, Tanmay co-leads clinical data and analytics solutions and focuses on using Medidata’s database of past clinical trials to solve complex problems in clinical development. Prior to joining Medidata Medidata AI, Tanmay was a management consultant at McKinsey and Company where he co-led the advanced analytics practice in North America.