Gary Pine

In this role, Gary leads W2’s product, marketing, design and innovation teams in Newport to develop and design the company’s products that are used by their clients millions of times every month. Prior to W2, Gary has worked in senior product roles for the likes of Bottomline Technologies, Autotrader and the Number 118118.

Mark Evans

Mark started his Marketing career in Mars Inc and for 10 years worked on a number of their global brands across sectors and geographies. Subsequently Mark worked at 118118 and then HSBC.

He joined Direct Line Group in 2012 in the build up to an IPO process and in the past 8 years has overseen the transformation of DLG’s brands and marketing approach, including the multi-award winning reinvigoration of the flagship Direct Line brand. Mark joined the DLG Executive Committee in 2019.

Mark is a Fellow of the Marketing Society and was voted the Financial Services Forum Marketer of the Year in 2015 and the Marketing Society Marketing Leader of the Year in 2018.

In 2016 Mark founded the Sprintathon in support of Stand Up To Cancer. The ambition is to Beat Cancer Faster by sprinting mass-relay marathons in schools and businesses.

Mark is Chair of the Advertising Association’s Front Foot and Non-Exec for LearnEtAl, an EdTech digital learning company

Jovonni Spinner

Ms. Jovonni Spinner is a public health strategist and thought leader with a deep passion for improving health equity across the lifespan through research, communication, multi-sector partnerships, and leadership coaching. She is known as a public health programming guru using her skills to direct projects from concept to fully operational through program design, implementation, monitoring and evaluation, and breaking down silos across sectors.

At the Food and Drug Administration, she is the Lead for the Outreach and Communications Team in the Office of Minority Health overseeing the strategic direction of the team, advising senior officials on minority health, and leading the Diversity in Clinical Trials Initiative. Prior to joining FDA, she managed national initiatives including the Community Health Worker Health Disparities Initiative, which aims to reduce cardiovascular and asthma health disparities through community education and training at the National Institutes of Health-National Heart, Lung and Blood Institute. She also provided health policy guidance to leaders on vaccine supply and finance policy issues at the HHS, National Vaccine Program Office, and served as the Director of Virginia’s Vaccines for Children Program ensuring the state’s Medicaid, uninsured, and underinsured populations were vaccinated.

She serves on non-profit boards; American Public University System and Society for Public Health Education, and writes women’s health articles for Health in Her Hue.

Ms. Spinner received her Bachelor’s degree in Biology from Virginia Commonwealth University, Master’s of Public Health from Emory University-Rollins School of Public Health and is pursuing her Doctorate of Public Health from Morgan State University.

Nirav Shah

Pharmaceutical professional with 20 years experience in managing global clinical supply chain activities including strategic planning and forecasting of clinical supply budgets, FTE’s, supply requirements and IRT development. Also responsible for managing and maintaining relationships with CRO’s, distribution vendors, suppliers, and packaging vendors.

John Benincasa

John is the Supply Chain Planner for Oral Solid Dose Manufacturing at Bristol Myers Squibb and is based at the New Brunswick, NJ facility. In this role, John manages Supply Plans as well as associated tasks, such as managing cross-functional Manufacturing Readiness Meetings, Capacity planning and ensuring starting material readiness.He is also the Supply Chain New System Implementation Lead. This role requires building system requirements, and test cases for UAT for new fully integrated planning system that will interface with production systems.

John has over 16 years of experience in the pharmaceutical industry, all within Clinical Supply Operations. He began his career as a Project Manager within this group and has held roles of increasing responsibility through the years.

John has a BS degree in Pharmacy from Philadelphia College of Pharmacy & Sciences and an MBA from Drexel University.

Alfredo D’Addio

Alfredo D’Addio – Director, Strategic Operations, Global Investigational Material Supply Chain at Celgene Corporation.

Over 14 years of experience in the Pharmaceutical industry in the area of Global Supply. A wealth of knowledge in the development lifecycle and interdependencies of the clinical supply chain to set strategies and proactively identify risks involved. Well versed with negotiation tactics to leverage partnerships/vendors, establish long-range objectives to develop strategies needed to achieve them. A solid background in forecasting & demand planning provides strong ability to identify gaps and implement solutions to gain efficiencies, while maintaining product quality. Thrives on setting short- and long-term strategies that proactively identifies challenges and implement solutions to minimize risk to the organization and to ensure patients have continuous access to therapies.

Bachelor of Science degree in Business Management at Fairleigh Dickinson University and has a Graduate Certificate in Pharmaceutical & Medical Device Law & Compliance from Seaton Hall School of Law.

Craig Mooney

Craig joined Calyx in 2021 as Vice President Scientific eTech Enabled Services, Craig has nearly 30 years of experience in the clinical trial arena including clinical operations, IMP packaging, labeling & logistics, with a primary focus in Interactive Response Technology (IRT). In his current role Craig’s remit is to: Leverage experience as an IRT business owner & sponsor to drive excellence in product, project management, and commercialization; Consult with clients on IRT best practices and emerging trends in the regulatory landscape; Serve as an advocate for sponsors within Calyx through expanded partnership engagements; And contribute to the industry as an evangelist for IRT and its proper role in clinical trials.

Judy Varga

Judy is a Nurse and has 20+ years in the Pharmaceutical Industry with various roles and for the past 7 years in  Biopharmaceutical and Medical Device Research & Development with Windtree Therapeutics, Inc.   She is currently overseeing the clinical team, closing 2 clinical trials and preparing for the next Phase 2 Clinical Trial that will hopefully launch into Phase 3 shortly thereafter.