Vivienne Marshall, Phd

Vivienne Marshall, Phd Email and Phone Number

Executive Director Starting Materials and Clinical Services BBG Advanced Therapies @ BioBridge Global
San Antonio, TX, US
Vivienne Marshall, Phd's Location
San Antonio, Texas Metropolitan Area, United States
Vivienne Marshall, Phd's Contact Details

Vivienne Marshall, Phd personal email

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Vivienne Marshall, Phd phone numbers

About Vivienne Marshall, Phd

Experienced Operations and Research Director with leadership in clinical, industry, academic, and non-profit settings. Skilled in Advanced Therapies; Clinical, Pre-Clinical, Translational, and Basic Research; Academic and Industry Grants Management; Biotechnology; Cell Culture; U.S. Food and Drug Administration (FDA); and Life Sciences. Skilled start-up expert. Strong research professional and proven leader, with a PhD in Embryology and Genetics from University College London, U. of London.

Vivienne Marshall, Phd's Current Company Details
BioBridge Global

Biobridge Global

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Executive Director Starting Materials and Clinical Services BBG Advanced Therapies
San Antonio, TX, US
Vivienne Marshall, Phd Work Experience Details
  • Biobridge Global
    Executive Director Starting Materials And Clinical Services Bbg Advanced Therapies
    Biobridge Global
    San Antonio, Tx, Us
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  • South Texas Blood & Tissue
    Executive Director, Center For Advanced Therapies
    South Texas Blood & Tissue Mar 2024 - Present
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  • South Texas Blood & Tissue Center
    Senior Director Center For Advanced Therapies
    South Texas Blood & Tissue Center Oct 2021 - Mar 2024
    San Antonio, Texas, United States
    Responsibility for Apheresis Services and Donor Management, Cord Blood & Birth Tissue collection, Deceased Donor Recovery and Hospital Relations, Donor Advocate Nursing, and Clinical Research.
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  • South Texas Blood & Tissue Center
    Director Of Clinical And Research Operations
    South Texas Blood & Tissue Center Nov 2020 - Oct 2021
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  • Canopy Growth Corporation
    Sw Usa Regional R&D Manager
    Canopy Growth Corporation Jun 2019 - Sep 2020
    San Antonio, Texas
    Management of national and international relationships and collaborations. Responsible for trial planning, protocol development, data management and interpretation, preparation of FDA regulatory materials, management of preclinical and clinical trials (domestic and international). Responsible for multiple research, formulation, and regulatory initiatives for a CBD product for the US companion animal market. Budget development and financial management.
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  • Baylor College Of Medicine
    Clinical Assistant Professor
    Baylor College Of Medicine May 2016 - Jun 2019
    San Antonio, Texas, United States
    Position held concurrently during 5-year tenure with Christus Health. Position involved education and support of clinical research faculty, including teaching and mentoring academic clinicians to grow research volume and increase restricted and unrestricted grant funding. Taught faculty and medical residents how to develop research study ideas into clinical research protocols, how to gain regulatory approvals, how to implement clinical research in a compliant manner, and how to complete and report study results in conference abstracts and peer-reviewed journals.
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  • Christus Health
    Regional Director Of Clinical Research
    Christus Health Jan 2016 - Jun 2019
    San Antonio, Texas Area
    Responsible for conduct and growth of clinical research at 5 hospitals in the San Antonio area, including The Children's Hospital of San Antonio (see below for description of concurrent position). Oversight of over 200 active research studies. Led development and advancement of both academic and industry sponsored research, including adherence to regulatory compliance, budget and contract development, financial oversight and revenue cycle for research. Management of external grant activities. Responsible for initiation and management of research billing process development for the Region that rolled out System-wide. Tier One leader.
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  • Christus Health
    Director Of Clinical Research At The Children'S Hospital Of San Antonio
    Christus Health Jun 2014 - Jun 2019
    San Antonio, Texas Area
    Initiated and led development of clinical research in the new Children's Hospital of San Antonio. Growth of over 200% in the first 12 months, and demonstrated 8-fold growth in 3.5 yrs. Complex research environment with multiple institutions including private practice physician groups, the clinical facility (Christus), and academic partner, Baylor College of Medicine. Led conduct and management of new institution's first industry-sponsored clinical trials, including contract, budget and regulatory management. Initiation and management of financial, clinical, educational, and compliance objectives for the new research enterprise. Successful grant submissions to Federal, State and Development offices. Co-organized highly successful annual research symposia for 4 years, welcoming pediatric researchers from all institutions in San Antonio. Tier One leader of 10 direct reports for 4 years. Interaction with community and media partners, and external affairs. Promoted to Regional Director at Christus Santa Rosa Health System in addition to this position.
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  • Rapamycin Holdings
    Senior Director, Medical Affairs
    Rapamycin Holdings Jun 2013 - Jun 2014
    San Antonio, Texas
    Responsibilities included: management of clinical trials including pharmacovigilance and data analysis and review; regulatory management of FDA submissions to both human FDA and veterinary FDA (Center for Veterinary Medicine); organization and tracking of patent and IP opportunities; writing and submission of new grant applications; consolidation and translation of scientific information into commercial development activities; facilitation of drug components for preclinical and clinical trials; and interfacing with commercial manufacturers and customers.
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  • National Trauma Institute
    Director Of Research
    National Trauma Institute Dec 2008 - Mar 2014
    San Antonio, Texas Area
    Developed and managed two national calls for clinical trauma research proposals, including development and issue of RFPs, the peer-review process of almost 200 proposals, the award of 16 selected clinical research studies for a total of $3.87 million, oversight of progress on the studies, and preparation of reports to funding agencies. The awarded clinical research studies involved 55 investigators nationally. Responsibilities included: compliance and program management of NTI’s congressional funding; seeking out, writing and preparing NTI’s extramural grant proposals, including pre-proposals and full proposals to both DOD and NIH; writing Congressional materials, including congressional special interest applications and Senate testimony; writing white papers and social media articles; and preparing other promotional materials. Worked regularly with NTI Board members and the Board Science Committee to maintain research progress and assist in the funding effort. Direct liaison with DOD contract and compliance specialists and scientists at USAISR, USAMRMC, USAMRAA, and TATRC.
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  • Noveome Biotherapeutics, Inc.
    Principal Investigator
    Noveome Biotherapeutics, Inc. Jan 2004 - Dec 2008
    Pittsburgh, Pa
    Responsibilities included: Writing and administration of multiple Department of Defense grants (total $3.25 million); Budgeting, compliance and reporting to DOD; Oversight of reimbursement and accounting/auditing per DOD requirements; Liaison with DOD contract specialists and scientists; Writing and submission of multiple SBIR grants; Management, writing and coordination of regulatory submissions including the company’s successful pre-IND, and IND submissions to FDA; Liaison with patent attorneys for writing and defending patent applications (25 patents granted); Co-ordination of all aspects of chemistry, manufacturing and control (CMC), within Stemnion and with outside vendors to ensure controlled management of the overall project; Reporting to CEO, and other management including Board Members; Staff recruitment and management; Promotion of the company to investors, politicians and other community leaders. Led the research and development of Stemnion’s first product candidate; development of business plans, budgets, staff recruitment and supervision, and lab set-up.
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  • Revivicor, Inc.
    Head Of Stem Cell Research
    Revivicor, Inc. May 2001 - Jan 2004
    Blacksburg, Va
    Project Leader for NIST Advanced Technology Program Grant, “Autologous Stem Cell Production”. Investigated technology for production of stem cells, without the use of embryos or fetal tissues, to be customized for individuals. Investigated means for transdifferentiation of cells directly from one cell type to another. Required establishment of a stem cell laboratory, direct supervision of technical staff, participation and consultation in other projects at the company, and liaison with senior management and grant funding bodies.
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  • University Of Wisconsin-Madison
    Research Associate At The Wisconsin National Primate Research Center
    University Of Wisconsin-Madison May 1995 - Dec 2001
    Madison, Wi
    Scientific research included isolation, culture and maintenance of non-human primate embryonic stem (ES) cells, and the first human ES cells; directed differentiation of primate ES cells; vector construction, purification and transfection into primate ES cells; development of a method for embryoid body production from primate ES cells to enrich for cell types of therapeutic use (patent granted); teratoma formation in immunocompromised mice; preparation of fibroblast feeder layers from mice; and pronuclear microinjection of rhesus monkey embryos. As a scientific lead of the Reproductive Research Services Unit, developed the first successful method for superovulation of marmoset monkeys and laparoscopic oocyte retrieval in marmoset monkeys; and performed laparocopic oocyte retrieval in rhesus monkeys. Supervised technical and animal care staff and co-ordinated efforts between staff in many groups, including continuous interaction with veterinary staff. Responsible for isolation, maintenance, culture and directed differentiation of marmoset and rhesus embryonic stem cells; direct microinjection of DNA into embryonic stem cells; culture of primate embryos; and blood sampling and hormone analysis of marmoset monkeys. Developed the first method for non-surgical embryo transfer in marmoset monkeys.
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  • Zoological Society Of London
    Phd Student
    Zoological Society Of London Aug 1990 - Mar 1995
    London, United Kingdom
    Thesis title: Manipulation of oocytes and early embryos of the common marmoset monkey (Callithrix jacchus). Developed a highly efficient method of parthenogenetic activation of primate oocytes and was the first to show development of parthenogenetic primate embryos beyond implantation. Conducted pronuclear transfer in primate and mouse embryos by micromanipulation; sperm collection and oocyte collection by surgical laparotomy in primates; in vitro fertilization and embryo transfer in mouse and marmoset monkeys; radioimmunoassays, ELISA, and bioassay; and artificial insemination of endangered species (Oryx, Gorilla, and Giant Panda). Supervised and coordinated efforts of technicians, veterinary and animal care staff.
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Vivienne Marshall, Phd Skills

Grant Writing Federal Grants Management Grant Administration Stem Cells Start Ups Genetics Biotechnology Regenerative Medicine Embryonic Stem Cells Differentiation Stem Cell Research Fda Embryology Research Primate Embryology Clinical Research Molecular Biology Lifesciences Cell Biology Cell Cell Culture Genomics Science In Vitro Grants Cancer Research Program Management Life Sciences U.s. Food And Drug Administration Clinical Trials Elisa

Vivienne Marshall, Phd Education Details

Frequently Asked Questions about Vivienne Marshall, Phd

What company does Vivienne Marshall, Phd work for?

Vivienne Marshall, Phd works for Biobridge Global

What is Vivienne Marshall, Phd's role at the current company?

Vivienne Marshall, Phd's current role is Executive Director Starting Materials and Clinical Services BBG Advanced Therapies.

What is Vivienne Marshall, Phd's email address?

Vivienne Marshall, Phd's email address is vi****@****wth.com

What is Vivienne Marshall, Phd's direct phone number?

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What schools did Vivienne Marshall, Phd attend?

Vivienne Marshall, Phd attended University College London, U. Of London, Massey University.

What skills is Vivienne Marshall, Phd known for?

Vivienne Marshall, Phd has skills like Grant Writing, Federal Grants Management, Grant Administration, Stem Cells, Start Ups, Genetics, Biotechnology, Regenerative Medicine, Embryonic Stem Cells, Differentiation, Stem Cell Research, Fda.

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