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Quantum Leap Healthcare Collaborative Welcomes Three Esteemed Leaders to Its Board of Directors

Dr. Janet Woodcock, Dorian Daley, and Keir Loiacano officially join April 24, 2025

San Francisco, CA – 4/28/25 – Quantum Leap Healthcare Collaborative (QLHC) is proud to announce the appointment of three distinguished leaders to its Board of Directors: Dr. Janet Woodcock, Dorian Daley, and Keir Loiacono. QLHC is a nonprofit specializing in innovative clinical trial design and is dedicated to better serving patients by accelerating and innovating health care through approaches that challenge the status quo of science and care.

These accomplished professionals bring decades of expertise in regulatory science, intellectual property, and biotech commerce, strengthening QLHC’s ability to advance cutting-edge research and improve patient outcomes.

Dr. Janet Woodcock – Former Acting Commissioner, U.S. Food and Drug Administration

Dr. Woodcock is a transformative force in clinical research and drug development, having spent over 30 years at the U.S. Food and Drug Administration (FDA). She played a pivotal role in modernizing drug evaluation and spearheaded key initiatives, including Operation Warp Speed during the COVID-19 pandemic. A longtime advocate of adaptive platform trials, she brings unparalleled regulatory insight that will be instrumental in advancing QLHC’s mission to streamline and optimize clinical trials.

“I’ve known Quantum and its work for many years, and I’m happy that I can now formally work with them on their revolutionary trial design, transforming clinical trial efficiency and effectiveness,” said Dr. Woodcock.

Dorian Daley – Former Executive Vice President and General Counsel, Oracle Corporation

As a seasoned leader in intellectual property and corporate governance, Daley will provide strategic guidance on QLHC’s innovative trial design and software assets. With a distinguished career at Oracle spanning over two decades, she brings expertise in compliance, ethics, and policy that will enhance the organization’s ability to scale and safeguard its groundbreaking work.

“I’m excited to be joining QLHC’s board alongside Dr. Woodcock and Mr. Loiacono. The hope and care QLHC gives to its patients, especially women, throughout the country is very inspiring. I’m glad I will be able to utilize my expertise and skills to drive QLHC’s IP for growth and impactful programs,” said Daley.

Keir Loiacono – Chief Executive Officer, BlueSphere Bio

As CEO of BlueSphere Bio, Loiacano actively navigates the complex landscape of drug development and deeply understands the need for collaborative relationships across multiple organizations to create change. He has over 20 years of experience in the biotech and pharmaceutical industry, bringing a distinctive perspective on accelerating novel therapies from discovery to market which aligns closely with QLHC’s commitment to getting better treatments to patients faster.

“I’m delighted to be in a position to serve QLHC. I understand the challenges of getting drugs from concept to market and the intricacies of the collaborations needed to achieve this. I look forward to helping to guide Quantum to get to the next level,” said Loiacano.

Combined, these three board members will provide scientific insight, advance intellectual property, and help amplify the growth and scalability of the organization and its programs. “We are honored to welcome Dr. Woodcock, Ms. Daley, and Mr. Loiacono to our Board,” said James Palazzolo, QLHC CEO. “Their collective expertise in regulatory science, intellectual property, and biotech commerce will help Quantum Leap Healthcare Collaborative drive meaningful advancements in precision medicine and patient-centered research.”

Full Board List Here

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More about each new Board Member:

Dr. Janet Woodcock – Former Acting Commissioner of the USFDA

Janet Woodcock recently completed a long career of over twenty years at FDA as the Director of the Center for Drug Evaluation and Research. In addition, she served as Principal Deputy Commissioner and prior to that as Acting FDA Commissioner. She held multiple other senior positions at FDA including at the Center for Biologics Evaluation and Research. She was the therapeutics lead for Operation Warp Speed during the COVID pandemic. Her most recent effort was spearheading a major reorganization of FDA’s foods program and the Office of Regulatory Affairs. Dr. Woodcock completed many major regulatory initiatives during her FDA tenure. She was instrumental in getting the biosimilars legislation enacted and worked to ensure adoption in the clinical community. Additionally, she worked with industry and Congress to bring about the first Generic Drug User Fee Act (GDUFA). After passage of the legislation, she oversaw an extensive reorganization of the generic drug review program at the Center for Drug Evaluation and Research (CDER) that successfully met the aggressive targets of the legislation and led to eventual reauthorizing, eliminating backlogs and approving thousands of generic drugs. Dr. Woodcock retired from FDA in 2024.

Dr. Woodcock has received numerous honors over her distinguished public health career, most notably: the Nathan Davis Award from the American Medical Association in 1999; the Roger W. Jones Award for Executive Leadership from American University in 2000; the VIDA Award from the Society for Hispanic Health and the first Leadership Award in Personalized Medicine from the Coalition for Personalized Medicine in 2005; the Garry Neil Prize for Innovation in Drug Development in 2009; a Lifetime Achievement Award from the Institute for Safe Medication Practices in 2015; the Florence Kelley Consumer Leadership from the National Consumers League in 2017; and the Biotechnology Heritage Award from the Biotechnology Innovation Organization and Science History Institute in 2019.

Dr. Woodcock holds a Doctor of Medicine from Feinberg School of Medicine at Northwestern University and a Bachelor of Science from Bucknell University. She also completed further training and a fellowship in rheumatology and held teaching appointments at Pennsylvania State University and University of California, San Francisco. She is board certified in internal medicine.

Dorian Daley – Former Executive Vice President and General Counsel, Oracle Corporation

Dorian Daley is the former General Counsel and Executive Vice President of Oracle Corporation, where she worked for three decades. Ms. Daley engaged with groups and management throughout the company and across the globe, navigating the complex and fast-paced business as it transformed from a database provider to a cloud computing and industry applications provider with a wide range of products and services.

Ms. Daley joined Oracle in 1992 as a member of the litigation and dispute resolution group. She later led that group as Vice President and Associate General Counsel before assuming the role of General Counsel in 2007. At that time, she also was named Corporate Secretary, a role she held for over a decade before appointing a colleague to the role. Ms. Daley also acted directly as Oracle’s Corporate Secretary Chief Compliance and Ethics Officer for several years. She retired from Oracle in 2022.

Ms. Daley has been the recipient of various awards and recognitions, including being named one of the Women Leaders in Tech Law, and singled out as one of 10 “Power Players”, lawyers who stand out as trailblazers, mentors, and advocates for women in technology, by the editors of The Recorder. In 2016, In 2016, Ms. Daley accepted the National Association of Women Lawyers Challenge Award in recognition of the significant representation of women in Oracle’s legal department and leadership roles; Ms. Daley was named as one of America’s 50 Outstanding General Counsel by the National Law Journal; and Ms. Daley’s legal department was named as one of the Best Legal Departments by Corporate Counsel Magazine. In February 2019, she was named as a “Legend of the Law”, awarded by the prestigious Burton Awards (in association with the Library of Congress), a national honor given to General Counsel whose careers in the law have been exemplary. 

Ms. Daley holds a Juris Doctor from Santa Clara University School of Law and a Bachelor of History from Stanford University.

Keir Loiacono – CEO of BlueSphereBio

Keir Loiacono is the current CEO of BlueSphere Bio and has nearly 20 years of experience from the biotech, pharmaceutical, and medtech industries. Prior to being appointed CEO, Mr. Loiacono served as Chief Business Officer for BlueSphere. Under his leadership, BlueSphere has grown into a clinical-stage cell therapy company with an initial focus on high-risk hematologic malignancies and a growing portfolio of differentiated assets. Before joining BlueSphere, Mr. Loiacono was the Vice President of Business Development and General Counsel of OncoSec Medical Inc., a public, clinical-stage oncology company. Earlier in his career, he worked as a senior director for Advaxis, Inc., a late-stage, publicly traded, immuno-oncology company focused on developing, manufacturing, and commercializing cancer vaccines, where he oversaw various legal, transaction, and compliance functions. Before Advaxis, Mr. Loiacono was an IP attorney with Lerner David Littenberg Krumholz & Mentlik, where he focused on transactions and building patent portfolios. For nearly a decade before this role, he held various commercial roles with OraPharma, a specialty pharmaceutical company that was purchased by Johnson & Johnson.

A patent lawyer by training, Mr. Loiacono represented companies of various sizes in all stages of transactions, including licensing and M&A, as well as complex corporate and governance matters. As a seasoned life sciences executive in the oncology sector, he has extensive experience raising capital in the public capital market space and closed numerous deals including licenses, clinical collaborations, and strategic transactions with significant upfront payments.

Mr. Loiacono holds a Juris Doctor from Elisabeth Haub School of Law at Pace University and a Bachelor of Science from Manhattan University.

About Quantum Leap Healthcare Collaborative

Quantum Leap Healthcare Collaborative (QLHC) is a 501c(3). It is nonprofit pioneer that designs, implements, and succeeds at building and iterating creative and nimble solutions that drive meaningful results for patients. Our mission is to better serve patients by accelerating and innovating health care through approaches that challenge the status quo of science and care. All our efforts focus on achieving our long-term vision to improve human health for all through personalized medicine by bridging the gap between research and care. QLHC provides operational, financial, and regulatory oversight to I-SPY. For more information, visit https://www.quantumleaphealth.org/.

Media Contact:

Jacqueline Murray

Director of Marketing and Communications

Quantum Leap Healthcare Collaborative

(415) 839-8082

j.murray@quantumleaphealth.org

Deborah Romer

Deborah’s breast cancer diagnosis in late 2022 catalyzed her interest in breast cancer research and patient advocacy following a complicated diagnosis. She is pleased to be participating as a patient advocate at UCSF, as well as with state, national and international groups, and has channeled her research and health care background in her advocacy work.

Deborah is a member of the National Breast Cancer Coalition and attended their Project Lead Science Training program in the summer of 2024, and will complete their Public Policy Institute in 2025. She serves on the Research Committee of the Lobular Breast Cancer Alliance (LBCA) and has been a grant reviewer for ASCO and LBCA. She begun working with Dr. Rita Mukhtar at UCSF on lobular breast cancer research and served on a panel for the Annual UCSF Breast Oncology Program Retreat. Deborah joined as a new member of the UCSF I-SPY Patient Advocate Panel in 2025 and serves as a Board member of Breast Cancer Care & Research Fund which links education, research and care to end breast cancer.

Throughout Deborah’s 30 plus year career in health care administration, she has worked to make health care more inclusive, accessible, equitable and personal. She started her health care career at the Stanford School of Medicine and then worked with several hospitals and health systems, including Kaiser Permanente where she worked for 22 years, serving as a medical group administrator and hospital CEO in Northern California, then at the National level as Vice President for Patient and Service Quality and as an Executive for National Quality and Board Governance.

Deborah is passionate about the importance of evidence-based research and multi-specialty team collaboration in solving problems and is committed to advancing breast cancer research, to supporting researchers, clinicians and patients, and to ensuring that the patients’ perspective is integrated into research, clinical trials and care. She has a BA with Highest Honors in Sociology and Research Methods from the University of California, Santa Cruz and a MBA from the Anderson School of Management at UCLA. She enjoys opera, jazz and the performing arts, as well as hiking, dancing and traveling, and is excited to be moving back to San Francisco in spring, 2025.

Tracey Heather

Advocate Liaison

As Patient Engagement Lead at Quantum Leap, I manage follow-up data projects for the I-SPY 2 Trial, develop strategies to strengthen patient engagement, and oversee the I-SPY Advocate group. After six successful years raising funds to support Quantum’s mission, I embraced this new role last summer, drawn by the opportunity to make a direct impact on the patients we serve. Each day brings new challenges and insights, and I especially enjoy supporting and collaborating with our inspiring I-SPY Advocates.

Outside of work, I am pursuing a Master of Public Administration with a focus on nonprofit management at SF State. I’m passionate about trail running, skiing, live music, camping, traveling, and collegiate gymnastics—my daughter competes at Oregon State. For the past 5 years, I have volunteered with SF CASA as a mentor to an incredible 18-year-old foster youth whose resilience continually reminds me of life’s true priorities.

Carolyn Clark Beedle

Carolyn Clark Beedle, a 2023 breast cancer survivor, joined the advocate program after successful completion of treatment with the UCSF Breast Oncology Program. Her experience working with a patient advocate during her TNBC treatment led to an understanding that empowering women to advocate for their own health and healthcare will contribute to improved health outcomes and broader access to care. Carolyn began advocating for cancer patients and their families during her treatment, now is a member of the Breast Science Advocacy Core (BSAC) with the UCSF Breast Oncology Program, and currently shares information and research with CFNP associates at La Clinica in the Bay Area to inform and empower their patient population.

Carolyn is continuing her on the ground training as an advocate reviewer with both Quantum Health and BSAC and is enrolled in the Patient Advocacy Training in Health Science course with Stanford Medicine. Her 30+ career in corporate marketing/communications, program development and non-profit leadership augmented by her breast cancer treatment experience serves Carolyn well in representing and communicating the patient voice and perspective.

She received her BA (History/English Lit) and MA (Public History/Research and Record Management) from the University of San Diego, is a proud fifth generation San Franciscan, and active board member with numerous non-profits that support social work and the arts.

Silver Alkhafaji

Silver Alkhafaji is a PhD candidate in the Pharmaceutical Sciences and Pharmacogenomics (PSPG) program at UCSF. She received her Bachelor of Science in Chemical Biology from UC Berkeley. Prior to UCSF, she worked in the Clinical Pharmacology Department at Genentech. Silver’s current research focuses on non-invasive liquid biopsies to predict response and side effects of immunotherapies and endocrine therapies in early-stage breast cancer participants in I-SPY 2.

Silver is interested in clinical outcomes research to advance precision medicine and improve cancer patients’ quality of life. She is passionate about health equity, inclusive research, patient advocacy, and women’s health.
Silver volunteers at the Patient and Family Cancer Support Center at UCSF where she assists in patient navigation and connecting patients and their families with resources that improve their healthcare experience while receiving cancer treatments and/or during survivorship. 

Through her DEI work in her PhD program, Silver raises awareness around issues related to social justice and community building through organizing community-centered events. Additionally, she is a member of the Life Sciences Career Advisory Council at Thrive Scholars, where she enjoys supporting college students of color from economically disadvantaged communities in providing the opportunities they need to thrive at top colleges and in high-trajectory careers. 

Silver is a member of the American Association of University Women (AAUW) Alameda Branch where she focuses her efforts on increasing membership of community college women coming from exceptional backgrounds: student parents, low-income, and first-generation college students.

In her free time, she writes poetry and prose on emotional healing, radical acceptance, and patience. Writing has helped her process difficult situations and connect with people on a deeper level.

Jane Mortimer

Jane is a breast cancer survivor and advocate dedicated to positively impacting the lives of women affected by the disease. Diagnosed with triple negative breast cancer in 2012, she participated in the I-SPY 2 trial at UCSF and has been cancer free for more than ten years.

Her advocacy journey began in 2003 at UCSF as a volunteer with the Patient and Family Cancer Support Center and Decision Support Services and she previously managed the Peer Support program at UCSF. Drawing on her experience in marketing and media strategy, she uses her skills to make a meaningful impact by supporting advocacy and research that improves outcomes for women living with breast cancer.

Jan Tomlinson

In March of 2023 , Jan was diagnosed with a large aggressive triple negative breast cancer and informed that her cancer was the” bad girl” of cancer and offered standard chemotherapy for 24 weeks. Devasted by the diagnosis Jan felt like she had a dire prognosis. After seeking several opinions, she opted to join a Clinical Trial program for her treatment. The trial consisted of significantly less chemotherapy, and monitored closely over a 12-week period, The data predicted a complete pathological response , and she then went immediately to surgery. Pathology reports supported that she had a successful outcome reaching PCR meaning the tumor was gone, and no residual cancer was found in the surrounding tissue or lymph nodes. Jan was thrilled when her surgeon advised her of the results. The experience made Jan want to give back and share information that she received when she was at a critical juncture in her diagnosis. She is so passionate about making sure that everyone knows that the standard of care is one treatment option.

As she says, “ clinical trials have to be on the table” Because she achieved PCR, she expects a great outcome. She wants to share her story and encourage other women to strongly consider and participate in clinical trials. Jan is a UCSF Patient Advocate, involved in several programs they lead. Jan also is a BLACC Cab Member. Jan recently was in Washington DC to participate on a panel on Clinical Trials for ISPY at the National Press Club. UCSF will be hosting the RISE Up For Breast Cancer event where Jan will share her experience with clinical trials.

Deborah Collyar

Deb is a connector who founded Patient Advocates in Research (PAIR) “where research meets reality,” bringing ideas and people together for medical advances that offer real results for diverse patients and families.

Her vast experience between the worlds of tech, communication, strategy, management, policy, and equity bridges gaps between patients, scientists, medical providers, payers, governments, and non-profits.

Deb infuses patient engagement into projects, gathers relevant patient input, and encompasses many diseases, programs and policies at grassroots, national and international levels through companies, academia, and governments.

Key patient insights are delivered throughout discovery, development, clinical trials, results reporting, data-sharing, standards, genomics, and into practice.

Her experience spans translational and clinical research, epidemiology, health outcomes, and health delivery research with academia, federal agencies, companies, and patient communities.