Thais Palma

Thais Palma

Intern

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location of Thais PalmaBrisbane, Queensland, Australia

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  • Timeline

  • About me

    CRA DP Manager & Onboarding Specialist at IQVIA

  • Education

    • Universidade Estadual de Campinas

      2007 - 2009
      Master's degree Basic Research
    • Universidade Estadual de Campinas

      2010 - 2014
      Doctor of Philosophy (PhD) Sciences
    • Vanderbilt University

      2012 - 2012
      Training as part of PhD, Urological Research Urologia

      CAPES Scholarship

    • Pontifícia Universidade Católica de Campinas

      2002 - 2006
      Bachelor's degree Pharmacy
  • Experience

    • Neofarma

      Jun 2003 - Aug 2003
      Intern

      Trainee at NeoFórmula (former Neofarma), pharmacy specializing in compounding since 1994, in the area of cosmetic compounding.

    • Apsen

      Jan 2004 - Feb 2004
      Intern

      Apsen is a 100% national company and operates in areas such as urology, rheumatology, ENT, neurology, geriatrics, psychiatry, gynecology, gastroenterology, pediatrics, gynecology, orthopedics and general medicine.Worked as a trainee at the Research and Development department. Followed all processes from product development to production and packaging.

    • EMS

      Sept 2005 - Jan 2006
      Intern

      Trainee in the department of Development of Analytical Methods, performing dissolution profiles, UV and HPLC analyzes and preparing spreadsheets and graphs with the results.

    • A Thriaga

      Jan 2006 - Feb 2006
      Intern

      With over 12 years of experience in compounding, A THRIAGA works with an extreme quality control of all products. Worked as a trainee, compounding homeopathic formulas.

    • Uptime Consultants

      Sept 2006 - Feb 2008
      English Teacher

      This first experience as a teacher was a key part of the professional development, where communication skills were developed, contributing to the academic maturity.

    • International Urogynecology Journal

      Jan 2008 - Aug 2017
      Reviewer

      Invited as part of the editorial review board of this international papers. The review process consists of evaluating articles that were sent for publication and providing feedback to help improve the level of the paper.

    • Universidade Estadual de Campinas

      Feb 2008 - Feb 2012

      Responsible for the development and submission of protocols to the Ethics Committee, administration, training staff, entering data into the CRF, reviewing documents. The State University of Campinas provides grad students with the opportunity to be a professor, under the guidance of their supervisors. In this period I taught med students of the 4th year in the Clinical Attention class.

      • Study Coordinator

        May 2007 - Feb 2012
      • Assistant Professor

        Feb 2008 - Nov 2011
    • In Touch

      Jan 2009 - Dec 2011
      English Teacher

      Worked as an English teacher for both children and adults of all levels. Other languages are not allowed in this school, so a lot of creative was of expression are encouraged, such as drawing or miming when necessary. Definitely the best was to learn and a fun place to be a teacher.

    • Neurourology and Urodynamics

      Feb 2012 - Aug 2017
      Reviewer

      Invited as part of the editorial review board of this international papers. The review process consists of evaluating articles that were sent for publication and providing feedback to help improve the level of the paper.

    • In Touch

      Jan 2013 - Aug 2013
      English Teacher

      Worked as an English teacher for both children and adults of all levels. Other languages are not allowed in this school, so a lot of creative was of expression are encouraged, such as drawing or miming when necessary. Definitely the best was to learn and a fun place to be a teacher.

    • EMS

      Sept 2013 - Jan 2016
      Clinical Research Associate

      Key participant in design and writing of protocols, case report forms and informed consent forms for clinical trials. Active participant in the design and implementation of clinical trials, preparation of integrated medical reports, periodic reports and Regulatory affairs. Assist in preparation of presentations and manuscripts of scientific meetings and technical journals. Attend scientific/professional meetings and training courses as appropriate.Also responsible for development and updates of SOPs and contracts. Show less

    • PAREXEL

      Jan 2016 - Apr 2016
      Clinical Research Associate

      Clinical Research Associate, providing clinical monitoring services to the Medical Affairs Department from Johnson & Johnson Family of Consumer Companies, outsourced by PAREXEL International.

    • Azidus Brasil

      Apr 2016 - Aug 2017
      Clinical Research Associate

      Monitoring for different sponsors, SOP updates, Linkedin and ResearchGate company profile updates, standardizing control spreadsheets for studies.

    • Journal of Obstetrics and Gynaecology

      Aug 2016 - Aug 2017
      Reviewer

      Invited as part of the editorial review board of this international paper. The review process consists of evaluating articles that were sent for publication and providing feedback to help improve the level of the paper.

    • IQVIA

      Aug 2017 - now

      The Onboarding Specialist Manages the activities relating to the Onboarding process for new hires in Site Management to ensure they are successfully integrated into the Company.Main activities include:Welcoming new hires, providing IT equipment and introducing them to the rest of the team;Overseeing the allocation of mentors to new employees;Assigning appropriate eSOP profiles and fast tracking the process of CV creation;Maintaining oversight and signing off of new hire training plans, including role specific and local training requirements;Supporting resources assignments and resource support plans;Completing accompanied site visits and making assessments for sign off for independent monitoring; Show less As a Senior Clinical Research Associate, main tasks include:Performing site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice;Supporting development of project subject recruitment plan;Providing monitoring visits and site management for a variety of protocols, sites and therapeutic areas.;Administering protocol and related study training to assigned sites and establishing regular lines of communication with sites to manage ongoing project expectations and issues;Evaluating the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations;Managing the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution;Providing assistance with design of study tools, documents and processesActing as mentor to other CRAs Show less

      • CRA DP Manager

        Feb 2024 - now
      • Onboarding Specialist

        Apr 2020 - now
      • Senior Clinical Research Associate

        Jul 2018 - Feb 2024
      • Clinical Research Associate

        Aug 2017 - Jul 2018
  • Licenses & Certifications

  • Honors & Awards

    • Awarded to Thais Palma
      Beca de Investigación Básica Confederación Americana de Urología Jun 2008 Bolsa de Investigação Básica pelo Projeto de Mestrado "Novo Modelo de Indução de Cistite Intersticial por Stress Oxidativo Utilizando Instilação Intravesical de Gel Doador de Óxido Nítrico".