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.