Laura González Rosales

I am a highly organized Clincial Research Coordinator & Project Manager with extensive experience in clinical trials and research projects. I have coordinated over 100 studies, including Horizon Europe and H2020 consortia, and bring strong expertise in managing workflows from start to finish.

I can cover project tracking, deadline follow-up, data cleaning and organization, biostatistical analysis (SPSS, R, Jamovi, JASP, excel), preparation of protocols, IRB forms, SOPs, databses (sharepoint, redcap, openclínica), datasets, tables, and appendices, manuscript formatting and submission to peer‑reviewed journals, and clear documentation with version control. I also provide regular updates and proactive solutions to delays.

My background is Master’s in Clinical Trial Monitoring, ongoing Master’s in Biostatistics, deep knowledge of regulatory frameworks (EMA, MDR, GCP), and hands‑on experience in clinical trial operations (phases I–III). I am also certified by BSI group in technical docummentation in MDR. Experienced in writing clinical trial protocols and clinical investigation plan, using mendeley, zotero, and good results in obtaining EECC, possitive opinion

Excellent English writing and communication, highly reliable, independent, and detail‑oriented.

I am available 10–20 hours per week depending on project volume.

As my professional background is head of R&D in a Spanish company with more than 20 clinics performing clinical trials simoultaneously over the years, I have trained myself to work across several projects simultaneously, turning complexity into structured workflows and reliable outcomes and enjoying in the process