Nour

Key Skills

Software

Other

Top Subject Matter

Clinical/pharmacological research documentation and experimental results evaluation

Clinical pharmacology research documentation and data interpretation (GCP-aligned)

Legal Services & Contract Review

Top Data Types

Document

Text

Top Task Types

Question Answering

Text Generation

Text Summarization

Transcription

Evaluation/Rating

Point/Key Point

Freelancer Overview

Drug Development Research Intern in Contract Review, Compliance, and Legal Research. Brings 1+ years of professional experience across complex professional workflows, research, and quality-focused execution. Core strengths include Other. Education includes Doctor of Pharmacy, Faculty of Pharmacy, Zagazig University (2027). AI-training focus includes data types such as Document and labeling workflows including Evaluation and Rating.

Labeling Experience

Undergraduate Research Assistant, Faculty of Pharmacy — GCP-aligned interpretation and evaluation of clinical research data (March 2026 - May 2026)

OtherDocument

Interpreted clinical research data related to oxidative stress mitigation and combined drug therapy efficacy and safety. Analyzed experimental findings to support evidence-based conclusions while adhering to GCP-aligned documentation practices. Performed protocol-consistent review and assessment of research datasets. • Assessed therapeutic efficacy and safety of combined drug therapies • Interpreted clinical data for oxidative stress mitigation • Analyzed experimental data supporting evidence-based conclusions • Ensured documentation aligned with GCP guidelines

2026 - 2026

Drug Development Research Intern (SRTA-City) — analytical data documentation and evaluation of assay results (Jan 2026 - Feb 2026)

OtherDocument

Documented analytical data according to SOPs, GLP, and basic GMP principles while working on pharmacological research activities. Interpreted experimental outputs to evaluate preliminary safety profiles and support evidence-based conclusions. Ensured scientific documentation alignment with regulatory-style requirements and study protocols. • Extracted and isolated bioactive compounds from natural sources for therapeutic applications • Conducted biological assays and recorded efficacy/safety-related results • Performed protocol-aligned documentation of analytical datasets • Followed SOP/GLP/GMP documentation standards

2026 - 2026

Education

Work History