Clinical Research Associate at Freelance (2026-01 – Present)
- Providing freelance start-up, monitoring and regulatory services to sponsors and CROs.
- Working in an international team including Clinical Project Managers and Line Managers.
Clinical Research Associate at TFS CRO - FSP (2024-11 – 2025-11)
- Performed site visits including site selection (SSV), site initiation (SIV), on site monitoring (SMV) and remote monitoring (REM) in Phase II and Phase III studies.
- Worked as blinded CRA and unblinded CRA in high priority studies.
- Worked with Risk-Based Monitoring Plans.
- General Monitoring Responsibilities
Clinical Research Associate at Syneos Health - FSP (2022-06 – 2024-11)
- Performed site visits including site selection (SSV), site initiation (SIV), site close out (COV), regular on site monitoring (SMV) and remote monitoring (REM).
- Performed recruitment support visits in order to enhance recruitment in non active sites.
- Worked as blinded CRA and unblinded CRA.
- Managed a maximum of 22 sites (6 unblinded) across different therapeutic areas.
- Experience with elderly and adolescent populations.
- Successfully attended an Sponsor Audit.
- Worked in an international team including Clinical Project Managers and Line Managers.
- Worked with top recruiting sites and high priority studies.
Clinical Research Associate at LabCorp - FSP (2021-11 – 2022-05)
- Performed Site Monitoring Visits and Remote Monitoring Visits for phase IV and phase II clinical trials (vaccines, oncology an rare diseases).
- Applied Risk-Based Monitoring.
- Experience with healthy volunteers population.
- General Monitoring Responsibilities
Clinical Research Associate & Study Coordinator at Hospital Álvaro Cunqueiro (2021-01 – 2021-11)
Clinical Research Associate and Study Manager in a Phase II Clinical Trial for COVID-19 involving several sites across Galicia.
- Designed of protocols, eCRF and ICFs, as Investigator Site File and Trial Master File, study documents templates.
- Prepared and reviewed all documentation for ethical evaluation.
- Conducted regular site visits (SMV), coordinated project meetings, and writing visit reports.
- Provided protocol training to sites at Investigator Meetings and site initiations visits (SIV).
- General Site Monitoring Responsibilities.
- Study Coordinator for 7 clinical trials in infectious diseases including Phase II and Phase III studies.
- Worked with the PI to develop and implement recruitment strategies
- Most recruiting site in Europe in a COVID-19 study.
- Successfully attended an Sponsor Audit.
- Assist investigators with local projects including Ethics Committee submissions, protocol drafts, local requirements, eCRF design at the Internal Medicine Department (e.g., HIV, thromboembolic disease…)
Country Study Specialist at Roche (2020-10 – 2021-01)
- Local Coordinator for several Compassionate Use programs in Oncology and Neurology.
- Managed new requests, including brief review of the eligibility criteria.
- Enrolled patients in Compassionate Use programs.
- Created and maintained program documentation.
- Sent medication to participating sites.
- Managed query resolutions with site personnel.
- Closed patient cases and sites.
- SIP (Shared Investigator Platform) Specialist: Guide investigators and teams in the use of the platform.
Clinical Trial Assistant at Grupo Español de Investigación en Sarcomas (GEIS) (2020-07 – 2020-10)
- Prepared and reviewed all documentation for ethical evaluation, submissions, contracts between GEIS and sites, as well as amendments.
- Contacted with sponsors, Ethics Committees, CROs, foundations and investigators.
- Provided advice to investigators, sponsors and CROs on administrative procedures (requirements, procedures, documentation) to be made in the presentation of evaluation applications to the CEIC.
- Experience in Observational Studies such as No-EPA, EPA-OD and EPA-SP in Oncology.
Clinical Trial Assistant & Clinical Reserach Associate Trainee at IQVIA - FSP (2019-09 – 2020-03)
- Supported CTAs and CRAs on daily tasks.
- Participated on Initiation Visit, Monitoring Visits, Remote Visit and pre-Closure Visits.
- Experience in Phase I-III clinical trials in several therapeutic areas such as Oncology, Cardiology, Hematology and Lung.
Pharmacovigilance Data Analyst at IQVIA (previously IMS) (2018-09 – 2019-09)
- Data Analysis and Quality Check of reportable safety information from patient data across various therapy areas following US and European Regulations.
- Applied CAPA system - root cause, corrective actions and preventive actions.
- Point of contact of Madrid team in an international project resolving queries from the other QCs and providing updates at the end of the day of each team member to the project manager.
- Quality Control Lead for international project solving pharmacovigilance doubts according with the clients guidelines.
