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Clinical Research Roundtable:
Envisioning a Truly Patient Centric Future in Virtual Clinical Trials
Tuesday, October 27, 2020, 11:30pm-1:00pm
Eastern US (Online, no charge)
Speakers:
Laurie A. Halloran, BSN, MS
President & CEO Halloran Consulting Group, Inc.
Laurie Halloran founded Halloran Consulting Group in 1998, originally operating out of an unfinished bathroom. Her time as a pediatric ICU nurse had inspired her to start a company that helps move new therapies through FDA processes to get them into the hands of patients desperately in need. By providing a strategic development team, innovative start-up companies could have access to world-class expertise at a fraction of the cost. Since its humble beginnings, Halloran has grown into a successful consultancy of like-minded experts who are dedicated to improving human health by making life science companies better at what they do.
Darshan Kulkarni
Principal Attorney of the Kulkarni Law Firm
Darshan focuses his practice on providing healthcare companies with comprehensive regulatory advice.
He previously served as Corporate Counsel for Nostrum Pharmaceuticals, where he was the first in-house attorney, built the company’s legal department, and oversaw all legal matters for the company. He has experience helping companies navigate privacy regulations such as GDPR and HIPAA when disclosing their clinical trial data and results. He also regularly counsels clients about balancing privacy concerns with patient transparency.
Most recently, Darshan served as Vice President of Regulatory Strategy and Policy at Synchrogenix, a VC backed global consulting company. He has spent over 20 years counseling clients on regulatory issues and has served as a pharmacist for over a decade. He has written several book chapters on regulatory compliance on behalf of the American Bar Association, where he is Chair of the Life Sciences Interest Group.
Clinical Research Roundtable
With frequent online sessions, this cohort explores Clinical Research from patient, sponsor, regulatory, and innovator perspectives.
Co-Chairs:
Daria Crean, RN
Clinical Research Operations Consultant
With a diverse, 30-year background as a champion of change, Daria actively implements her creative and innovative ideas in clinical research. Her ongoing focus is the constant need for bridging the gap between clinical practice and research during this evolving time.
She has built deep understanding and knowledge through a variety of roles and settings. As a clinical operations consultant at Huron Consulting Group, she initiated the rebuilding infrastructure of clinical research programs. At a US-based CRO she created successful model for Phase III medical device trial sites as a patient recruitment specialist.
Ellen Bedenko, RN, CCRC
Clinical Research Coordinator
Temple University Heart Failure Research Program; Temple Cardiorenal Biorepository
Ellen Bedenko is a seasoned clinical research professional with knowledge and perspectives on the clinical trials process developed while working at sponsor, CRO, and vendor levels.
Her areas of interest are patient recruitment and retention, inclusion of patients with limited English proficiency, inpatient clinical trials, and biobanking for both investigator-initiated and industry-sponsored trials.
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