Marian Markovic

Background

About Marian Markovic

Deputy Scientific Director with 9 years of experience in Biomarker assay development, validation and sample analysis for clinical trials. Skills in LBA (ELISA/MSD), Flow Cytometry, Biosimilars, GLP/GCP/GCLP, regulatory guidelines, Pharmacokinetics, Immunogenicity, Pharmacodynamics, study and project management. • Assay Validation Expertise: Strong background in developing and validating ligand-binding assays to support pharmacokinetics, biomarkers, and immunogenicity assessments for preclinical and clinical studies. • Scientific Leadership: Contribute bioanalytical expertise to cross-functional project teams, actively participating in discussions and presenting findings at internal multidisciplinary meetings. • Clinical Trial Support: Proficient in monitoring bioanalytical study phases, reviewing sample analysis/validation plans and reports, and contributing to clinical trial documentation (protocols, data transfer agreements, lab manuals). • Experimental and Operational Oversight: Hands-on experience in performing experimental work during assay development/validation while ensuring scientific rigor, data completeness, and regulatory compliance. • Client Collaboration: Adept at understanding client-specific assay requirements and delivering custom assay solutions in compliance with regulatory standards. • Project and Team Management: Proven ability to lead teams, meet project deadlines within budget constraints. Experienced in mentoring bioanalytical scientists and supporting their professional development.