Mariela Gangemi

Experience

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  Laboratory of Defects in Axonal Transport and Neurodegenerative Diseases

  Dec 2009 - Apr 2010

  Intern

  Fluorescence Microscopy, Western blottingMolecular Biology (DNA extraction, Gel Electrophoresis)

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  Laboratory of Agrobiotechnology

  Aug 2010 - Mar 2012

  Undergraduate Thesis Candidate

  Development of transgenic and mutant plant viruses to study cell-to cell viral movement. Cloning and biochemical characterization of movement proteins. Molecular Biology Techniques (PCR, DNA extraction, Gel Electrophoresis), Molecular Cloning and Genetic Engineering, Agrobacterium tumefacines-mediated genetic transference in plants. Reading and analysis of scientific articles in English.

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  Laboratory of Molecular and Cell Therapy

  Apr 2012 - Feb 2014

  PhD Candidate

  Development of Conditionally Replicative Adenoviruses to treat ovarian and cervical cancer. Testing of the drug in cell culture, mice and human tumor samples. HPV-testing of tumor samples. Molecular Biology Techniques (PCR, Real-time PCR, DNA and RNA extraction, Gel Electrophoresis), Molecular Cloning and Genetic Engineering, Cell culture, Microscopy, Viral culture and purification. Work conferences and seminar presentations. Administration of antibodies of use in the laboratory. Reading and analysis of scientific articles in English. Show less

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  PAREXEL

  Mar 2014 - May 2017

  • Remote Monitoring for Clinical Research Studies. Therapeutic Area: Oncology, Lung Cancer, Phase III Clinical Trial for United States and Canada. The responsibilities of a Clinical Monitoring Associate (CMA) II include:• Performing remote clinical monitoring tasks and remote visits for designated projects in accordance with relevant SOPs, study specific procedures and regulations. • Managing/coordinating/supporting clinical monitoring activities remotely, including issue resolution, patient enrollment management, handling protocol and/or ICF and/or contract amendments, drug supply/ management and ensuring timely data entry at a site level.• Participating in study-specific and corporate trainings.• Mentoring other CMAs that have recently joined the company in the role and responsibilities. Show less Remote Monitoring for Clinical Research Studies. Therapeutic Area: Oncology, Lung Cancer, Phase III Clinical Trial for United States and Canada. The responsibilities of a Clinical Monitoring Associate (CMA) I include: • Performing remote clinical monitoring tasks and remote visits for designated projects in accordance with relevant SOPs, study specific procedures and regulations. • Managing/coordinating/supporting clinical monitoring activities remotely, including issue resolution, patient enrollment management, handling protocol and/or ICF and/or contract amendments, drug supply/ management and ensuring timely data entry at a site level. • Participating in study-specific and corporate trainings. Show less

  • Clinical Research Associate II

    Nov 2016 - May 2017

  • Clinical Research Associate I

    Aug 2015 - Oct 2016

  • Clinical Monitoring Associate II

    May 2015 - Jul 2015

  • Clinical Monitoring Associate I

    Mar 2014 - Apr 2015
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  PRA Health Sciences

  Jun 2017 - Jul 2019

  Clinical Research Associate II

  Providing monitoring services to Sanofi.

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  PRA Health Sciences

  Aug 2019 - Jan 2020

  Senior Clinical Research Associate

  Providing monitoring services to Sanofi.

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  ICON plc

  Jul 2022 - Nov 2024

  Local Study Manager
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  Sanofi

  May 2024 - now

  Clinical Project Leader