Maddi Arsuaga
Clinical Research Associate II at SOLTI- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
-
Español -
-
Basque -
-
English -
-
Basic French Level -
-
Good Catalan understanding -
Topline Score
Bio
0
/5.0 / Based on 0 ratingsFilter reviews by:
Credentials
-
Handling mice: Small interventions and treatments
Max Delbrück CenterFeb, 2015- Sep, 2024 -
Experimental animal user
Universitat de BarcelonaJan, 2015- Sep, 2024 -
IELTS Certificate in English: 7.5
British CouncilJan, 2015- Sep, 2024 -
Cambridge English: Advanced (CAE)
Cambridge English Language AssessmentJan, 2010- Sep, 2024 -
Good Clinical Practice, Version 5, effective 03-Mar-2017
NIDA Clinical Trials NetworkApr, 2020- Sep, 2024
Experience
-
SOLTI
-
Spain
-
Research
-
1 - 100 Employee
-
Clinical Research Associate II
-
Sep 2020 - Present
-
-
-
none
-
Information Technology & Services
-
1 - 100 Employee
-
International Volunteering
-
Sep 2018 - Mar 2020
Eighteen months of travel to Latin America. Activities included a wide range of volunteer work such us teaching in an Amazonian community, helping managing hostels and community based tourism agencies and acting as an English translator. These experiences have contributed to my personal growth and strengthen my negotiation and people skills. They have also helped me develop a flexible, diverse and empathic mindset and taught me to confront unexpected and complex situations relying on my own decision making. Show less
-
-
-
Theradex®
-
United Kingdom
-
Biotechnology Research
-
1 - 100 Employee
-
Clinical Research Associate
-
Jan 2016 - Jun 2018
- Monitored phase Ib, II and III clinical trials in accordance with GCPs. - Provides site management and monitoring support for sponsored clinical studies. - Conduct Site Qualification, initiation visits, on-site monitoring visits and co-monitoring visits of clinical trials. - Prepare site visit reports and provide assistance to site staff in resolving deficiencies. - Educates and trains site and study staff in conduct and management of sponsored studies, including assurance to regulatory and ICH/ GCP compliance. - Collects and processes regulatory documentation for investigational studies in compliance with required guidelines. - Develops and demonstrate an understanding of and apply therapeutic area knowledge to assignments and project-related issues. - Appropriately resolves issues related to trial monitoring and management with guidance from Project Manager. - Assisted Project Director in the execution of the daily operations in managing the development of drug candidates. - Recruited and evaluated potential investigators. Show less
-
-
-
Charité Berlin
-
Germany
-
Business Consulting and Services
-
Master Thesis Student
-
Feb 2015 - Aug 2015
- Designing and performing biomedical experiments for the study of the Graft versus Host Disease in multiple and single minor antigen mismatched murine models using in vivo bioluminescence imaging. - Using specialised information technology to accurately record and analyse data, write reports and share results. - Presenting ongoing work and findings to colleagues, and summarising the nature of the research, methodology and results. - Implementing quality control procedures to maintain accurate results. Show less
-
-
-
Max Delbrück Center
-
Germany
-
Research Services
-
500 - 600 Employee
-
Bachelor Thesis Student
-
Mar 2014 - Aug 2014
- Development of animal cellular assays to investigate the characterization of the putative immunoregulatory protein Rab33A in murine T cells. - Performing laboratory tests in order to produce reliable and precise data to support scientific investigations. - Carrying out fieldwork: collecting samples and monitoring environmental factors. - Recording and interpreting results to present to senior colleagues. - Using specialised programs and performing mathematical calculations for the preparation of graphs. - Constructing, maintaining and operating hi-tech laboratory equipment such as microscopes, centrifuges, fume hoods, pipetting machines and pH meters and ensuring the laboratory is well-stocked and resourced. - Following and ensuring strict safety procedures and safety checks. Show less
-
-
Education
-
Universitat de Barcelona
Bachelor of Science (BSc), Biochemistry -
Universitat de Barcelona
Master of Science (MSc), Biomedicine -
UNIR - La Universidad en Internet
Online Certificate Program in Clinical Trial Project Management, 8.3 Notable