Alia Shafiq

Led planning, design and coordination of clinical and observational studies for dermatology and nutraceutical products, ensuring GCP/EFSA/EMA compliance and timely delivery of study reports and conference materials.

Operationally managed clinical and medical projects in gynecology and obstetrics, coordinating multicentre NIS and IITs and overseeing protocol/CRF development, ethics submissions and budget tracking.

Supported design and coordination of multicentre clinical studies in hematology and pediatric endocrinology, conducted site qualifications and ensured regulatory and GCP compliance across sites and CROs.

Developed and executed strategic brand plans for rare disease products, supported launches and lifecycle management, and managed budgets, training materials and scientific content using CRM and promotional systems.

Assisted coordination of investigator-initiated and non-interventional studies across EMEA, supported ethics and regulatory document review and contributed to central file management and audit readiness.

Participated in biomedical research projects in physiology, pathology and molecular diagnostics as part of a biotechnology degree final project, contributing laboratory support and data collection.

Completed an MBA focused on the pharmaceutical industry, covering strategic and operational aspects relevant to pharma business roles.

Completed a Master in Molecular Oncology with coursework and research in molecular mechanisms of cancer.

Completed a specialization in clinical trials and pharmaceutical development covering trial design, regulations, and operational processes.

Earned a Bachelor's degree in Biotechnology with laboratory research experience culminating in a final project in physiology, pathology, and molecular diagnosis.