ATIA SHEEREEN

• Coordinated multiple cancer trials, including prostate, head and neck, skin, and lung studies.
• Increased participant screening and recruitment by at least 20% as lead trial coordinator.
• Conducted patient screening and genomics-based eligibility assessments to enhance recruitment efficiency.
• Managed visit scheduling, CRF entry, and query resolution to ensure trial integrity.
• Prepared and submitted annual reports and amendments to HREC and Governance bodies.
• Supported PhD biomarker studies by generating stickers and creating blood collection research kits.

• Led 13 clinical trials and co-managed 10, achieving key project milestones.
• Oversaw informed consent processes, genomics screening, randomization, drug ordering, and participant retention.
• Managed data using EDC systems including Rave, BaCT-Viedoc, RedCap, and InFORM 6.0.
• Maintained ALCOA-compliant data and submitted ethics reports for regulatory compliance.
• Coordinated international travel arrangements for trial participants to improve accessibility.
• Served as Lead CRA for Firefly-1 and Firefly-2 trials, achieving 20% recruitment growth.
• Developed training materials that increased staff compliance by 35% across trials.
• Enhanced follow-up compliance by 40% in 15 COG trials through targeted strategies.

Coordinated familial hemophagocytic lymphohistiocytosis (FHL) study to advance research initiatives.

• Discovered novel gene mutations and compiled comprehensive mutation reports.
• Validated DNA sequencing results, contributing to multiple co-authored publications.

• Executed advanced molecular techniques, including PCR, RT-PCR, Western blotting, and sequencing.
• Managed informed consent processes alongside clinical data collection for participant tracking.
• Trained junior staff to uphold rigorous lab documentation standards.
• Contributed to seven peer-reviewed publications that advanced scientific knowledge in the field.