Ecem Yavuz

• Support new project research, feasibility analysis, and resource evaluation.
• Coordinate cross-functional activities across Planning, Regulatory Affairs, Clinical, Bioequivalence, and
technical teams.
• Track project milestones, timelines, risks, and required actions throughout the product lifecycle
• Support clinical research documentation and regulatory submissions

• Assisted in laboratory analysis of hospital-derived blood samples.
• Contributed to Western blot and in vitro enzymatic assays.

• Prepared and reviewed regulatory submission documents.
• Monitored regulatory updates, submission timelines, and approval processes.
• Reviewed product labeling and patient information materials for compliance.

• Reviewed patient files and supported clinical evaluations.
• Participated in patient education and clinical documentation.

• Gained experience in patient communication, prescription management, and pharmacy operations.