Elizabeth Tarshish

Experience

• 

  Hadassa Medical centers the hebrew university jerusalem

  Jan 2001 - Jan 2008

  Pre-Clinical Research

  2007-2008 Hepatology Department (Hadassah Hospital)-2004-2007- Cardiology Department (Hadassah Hospital, Jerusalem) 2003-2005 - Laboratory of Transgenic Animals (Hebrew University Medical School) 2003-2004 - Anatomy Department (Hebrew University Medical School) 2001-2003 - Oncology Laboratories (Hadassah Hospital, Jerusalem)

• 

  Quark Pharmaceuticals Inc

  Jan 2008 - Jan 2010

  In vivo modeling/ Preclinical Data base appointee

  Preclinical Database appointee- data collection and processing.In vivo unit assistantnt

• 

  BioLineRx

  Jan 2010 - Jan 2013

  Senior Clinical Research Associate/ Project Manager

  • Management and startup of global clinical studies worldwide- Phase 1 to 4.• Management of clinical sites, CROs, and CRAs.• Pharmacovigilance activities and reporting. • Management and fulfillment of study activities- patient recruitment, initiation, adherence to local regulation and study requirements, study supplies, monitoring

• 

  Novartis

  Jan 2010 - Jan 2010

  Clinical Trial Associate

  • Interaction and coordination with sponsors, SC, Sites, Vendors• Preparation and submission of applications and all related documentation to the ethical Committee and local health authorities, revision of regulatory documents.• Overlooking enrolment and execution of clinical studies

• 

  IMMUNE Pharmaceuticals Ltd.

  Jan 2013 - Jan 2015

  Clinical Operations Manager

  • Managing and overseeing operational aspects, including clinical activities, protocol planning, patient care, resources distribution, business activities, and coordination of project teams of local and global clinical trials phase 2-4.• Clinical writing and document origination (protocols, amendments, CRF, informed consent forms, etc.).• Budget planning and execution

• 

  Teva Pharmaceuticals

  Jan 2015 - Jan 2017

  Senior Clinical Project Manager

  • Managing and overseeing operational aspects of global clinical trials - Phase 1 to 4. • Planning and feasibility assessments of projects.• Cross-function integration -business infrastructure, data management, and medical affairs, etc.• Support in achieving project deliverables within scope, budget, and timelines.

• 

  Lycored

  Jun 2017 - now

  Established and implemented standards to support the portfolio from new product development ideation to launch. Facilitated cross-functional collaborations with Marketing, Regulatory, and R&D teams, leading to the creation of a new pipeline.Sales and Marketing Integration with Scientific Communication:Train sales and marketing teams on the product portfolio and serve as the company spokesperson at public, industry, and scientific events. Additionally, play a key role in developing marketing campaigns to enhance brand awareness and showcase the company's scientific expertise. Show less Science and Innovation Strategy:Directed the science, innovation, and claims pipeline by overseeing pre-clinical and clinical trials, obtaining patents, and publishing peer-reviewed articles. These initiatives significantly enhanced the value proposition and opened new market segments, highlighted by the development of claims that led to a pivotal strategic partnership.Leading Science Commercialization Strategy:Transforming scientific results into marketing materials and tools by crafting unique value propositions and claims that align with market trends. Show less As a Clinical Study Director, I led the end-to-end management of clinical trials, from initial study design through to data analysis and publication. I collaborated closely with cross-functional teams—including regulatory, scientific, and marketing departments—to ensure studies were aligned with both strategic objectives and regulatory standards. My role involved designing rigorous study protocols, overseeing participant recruitment, and ensuring adherence to GCP (Good Clinical Practice) guidelines. I also managed relationships with external research organizations and investigators, coordinating timelines and resources to achieve high-quality, reliable results. Additionally, I analyzed and interpreted complex clinical data, transforming insights into actionable outcomes that supported product claims and guided business strategies. My leadership in these trials not only drove innovation but also reinforced the scientific credibility and market differentiation of our products. Show less

  • Head of Product and Science

    Nov 2024 - now

  • Head of scientific affairs and claim substantiation

    Jun 2021 - Oct 2024

  • Clinical studies Director

    Jun 2017 - Jun 2021