Andja ÇARÇIU

Coordinated scheduling, logistics, and stakeholder communication for a life sciences training program. Liaised with healthcare professionals and trainers to ensure smooth delivery and timeline adherence. Managed and maintained structured documentation, ensuring accuracy and accessibility. Monitored timelines, participation, and feedback, supporting reporting and process improvement in a multidisciplinary environment.

Performed ELISA-based ADA and titration assays to evaluate antibody candidates against SARS-CoV-2 variants. Conducted pseudovirus neutralization assays and site-directed mutagenesis within structured workflows. Ensured accurate data documentation, integrity, and sample traceability in a GLP-compliant environment. Supported assay qualification and SOP development, contributing to standardized processes, improved reproducibility, and cross-functional collaboration.

Performed ELISA testing within a national surveillance program, supporting regulated research activities. Conducted virus detection targeting gE and gB glycoproteins using standardized methods. Supported epidemiological surveillance through sample identification, tracking, and data handling. Ensured accurate documentation and quality-controlled reporting, and contributed to peptide mapping (PEPscan) projects aligned with research objectives.

Performed laboratory techniques (Western blot, cell culture, PCR, FACS) following established protocols and quality standards. Maintained accurate, traceable, and audit-ready records to ensure data integrity and transparency. Supported oncology research using tumor cell models, contributed to experimental planning, and coordinated daily lab activities. Ensured SOP compliance and maintained high standards of documentation and organization.

MSc in Molecular Biology with experience in biotech and public health research, including work in GLP-regulated laboratories. Skilled in molecular biology techniques, experimental workflows, and structured documentation. Trained in clinical research (GCP, pharmacovigilance, study design). Detail-oriented and reliable, with experience supporting multidisciplinary teams, data integrity, and project-related activities in regulated environments.