Paula Anglada Email & Phone Number

Barcelona, Ct, Es

Barcelona, Ct, Es

Barcelona, Catalonia, Spain

Working in Consumer Healthcare Pharmacy Department providing support in different tasks:- Scientific literature review: searching, reviewing, and summarizing relevant scientific literature for the company's pharmaceutical products.- Participation in the development of scientific materials: creating educational and scientific materials aimed at healthcare professionals, such as monographs, presentations, and informational bulletins.- Assistance in organizing medical events: planning,… Show more Working in Consumer Healthcare Pharmacy Department providing support in different tasks:- Scientific literature review: searching, reviewing, and summarizing relevant scientific literature for the company's pharmaceutical products.- Participation in the development of scientific materials: creating educational and scientific materials aimed at healthcare professionals, such as monographs, presentations, and informational bulletins.- Assistance in organizing medical events: planning, coordinating, and executing medical events, such as symposiums, conferences, and meetings with KOLs.- Support in responding to medical inquiries: assisting in responding to medical inquiries from healthcare professionals about the company's pharmaceutical products, providing accurate and updated information.- Participation in clinical research projects: Collaborating on clinical research projects, including protocol review, study progress monitoring, and communication with investigators.- Contribution to external and internal medical training: development and delivery of continuous medical education programs for both healthcare professionals and company employees on the company's products and their scientific bases. Show less

Barcelona, Catalonia, Spain

During my stay I worked developing the following tasks:- Recording transactions in sponsor systems (IWRS) as well as patient data in research applications.- Realization and implementation of coordinated procedures between the different clinical services involved in the inclusion, treatment and follow-up of patient participation.- Completion of CRFs, resolution of queries,- Reporting of SAEs.- Communication with Sponsors and CROs.- Preparation and attention to monitoring… Show more During my stay I worked developing the following tasks:- Recording transactions in sponsor systems (IWRS) as well as patient data in research applications.- Realization and implementation of coordinated procedures between the different clinical services involved in the inclusion, treatment and follow-up of patient participation.- Completion of CRFs, resolution of queries,- Reporting of SAEs.- Communication with Sponsors and CROs.- Preparation and attention to monitoring visits, initiation and closure visits.- Transferring of study data to the CRF, registering data and keeping updated all the clinical trial tools.- Keeping updated the study files.I gained experience working on the following Clinical Trials:Phase III – Breast Cancer TrialsPhase II – Gynecological Cancer TrialsPhase II – Head and Neck Cancer Trials Show less

Barcelona, Cataluña, España

I have given my support in different areas of the clinical trials design: - Development and management of key study documents defining the design and procedures required during clinical trials.- Biological samples collection management, including shipments tracking, processing oversight and sample conciliation, for translational analysis.- Databases management and data validation processes.- Contribute to results reporting for clinical trials.- Participation in team… Show more I have given my support in different areas of the clinical trials design: - Development and management of key study documents defining the design and procedures required during clinical trials.- Biological samples collection management, including shipments tracking, processing oversight and sample conciliation, for translational analysis.- Databases management and data validation processes.- Contribute to results reporting for clinical trials.- Participation in team communications and meetings. Show less

Master In Pharmaceutical And Biotechnology Industry, Pharmaceutical Industry

Bachelor'S Degree, Biomedical Science

Erasmus+ Programme, Bachelor Of Biomedical Science, General

Courses hold in italian and english

Big Data And Business Intelligence

High School Diploma, Graduated With Honors