Sarah Moussa

• Coordinated site and operational activities for over 15 global oncology trials (Phase I–IV), from study start-up through close-out, ensuring full compliance with GCP, SOPs, and study protocols.
• Acted as a main point of contact for clinical sites and sponsors, addressing queries and resolving discrepancies to keep trial databases accurate and up to date
• Managed CRO deliverables and imaging QC data tracking, consistently meeting submission deadlines and maintaining high-quality imaging standards.
• Led site qualification and training for new site staff, ensuring each site was fully prepared and equipped to conduct all phases of the study.
• Reviewed and resolved data issues flagged by clinical data management, helping to speed up discrepancy resolution times and keep studies on track.

Reviewed and tracked all data from clinical sites to ensure accuracy.

Conducted training for new members, providing feedback on task completion.

Applied data privacy policies to maintain compliance with sponsor requirements.

Monitored data submissions to confirm expectations based on project protocols.

Supported protocol revisions, resulting in enhanced accuracy and completeness within the team.

Conducted quality control tests on ingredients and equipment to ensure effectiveness and safety.

Accurately recorded over 200 sets of results in compliance with Standard Operating Procedures.

Developed a suite of reporting tools for tracking progress against key performance indicators.

Maintained effective customer service through telephone and email communication with clients and external teams.

• Performed routine and non-routine calculations, creating visualisations using Microsoft Excel.