Mariana Queiroz

I’m a Pharmacist with a strong interest in Clinical Research. My academic and professional background are in Pharmacy, Regulatory Affairs and Clinical Trials, which gives me a broad vision of drug development. Excellent organizational, team work and problem-solving skills, I want to use my abilities to push forward well design clinical studies and contribute to improve quality of life of patients.

Aug 2022 - Present

Roche - Switzerland

Working closely with Study Lead, overviewing study conduct and managing the study team.

Conduct of meetings with CRA and CRO to insure milestones are achieve and GCP compliance.

Experience with systems and documents like CTMS, IxRS, eTMF and CRF.

Jan 2022 - Aug 2022

Silva Tavares Laboratory - Portugal

Managing clinical analysis laboratory

Collecting blood samples from patients and delivering results

Training new staff according to GLP

Feb 2019 - Mar 2020

VITA Regulatory Affairs Consultant - Portugal

Assisting in the analysis of Drug Master File of companies that wanted to place their product in a different market and giving them regulatory opinion before submission.

Articles publications on LinkedIn and in the company's website about news from

Regulatory Agencies (EMA, FDA and ANVISA).

Sep 2020 - Mar 2023

Master degree in Regulation and Evaluation of Medicines

Master thesis ''Efficacy and Safety of Covid-19 vaccines: the adaptive pathways for EU approval''

During my master I got the opportunity to increase my knowledge in ethical aspects of patient recruitment for clinical trials, randomization, ICH Guidelines and regulatory aspects of clinical trials

Sep 2012 - Dec 2017

Federal University of Paraná - Brazil

Bachelor in Pharmacy

Award for "Best work presented" with the research Lipid and Glucose Dosage in

Adolescents of the State Schools in Curitiba PR.