Hanin Atia

Pure Health is the largest integrated healthcare network in EMEA with portfolio of 100+ hospitals, 200+ clinics, 170+ laboratories, a digital CRO, and an insurance company across the UK and USA.

• Oversight and management of clinical operational activities across the international region (i.e., contracts, budgets, invoice management, etc.).
• Leading,Planning and Project management activities across the network and ensuring integration with global activities.
• Establishing performance indicators for research and generate status reports to keep stakeholders informed.
• Tracking performance through goal setting and tracking, monthly and quarterly metric reports and analytics dashboards.
• Identifying, contracting, managing and monitoring third-party vendors to perform activities in the region.
• Developing and implementing business process and SOP development, as well as ensuring training and process improvement of business tools.
• Partnering with IT to develop and implement software solutions/data platforms to support business needs.
• Developing, tracking and managing budget forecasting, long-range planning and tracking operational expenses.
• Planning and developing regional training and onboarding plans from a functional perspective.
• Analyzing P&L statements and evaluating the financial performance.
• Leading the group AAHRPP accreditation.

Responsible for (14) studies in phases (1) and (3), oncology, Hematology, and Neurology.

• Managed a complex lymphoma phase I study and supported the US team.
• Coordinated with cross-discipline team members to ensure all parties were on track with project requirements, deadlines, and schedules.
• Managed Phase I-III clinical trial activities from planning through to closeout, ensuring all metrics are met.
• Managed trial documentation.
• Submitted project deliverables and ensured that they adhered to quality standards.
• Facilitated change requests to ensure that all parties were informed of the impacts on schedule and budget.
• Ensured that all staff implemented and followed all Standard Operating Procedures (SOPs) and Policies.
• Oversees resourcing allocations.
• Successfully delivered on tasks within tight deadlines.
• Stakeholder management.

• Trained and mentored junior team members, leveraging previous experiences in boosting project progress.
• Monitored IP dispensation and administration, overseeing (re) labeling, importations, releases, and returns.
• Improved operations by generating project status reports and identifying issues for corrective action.
• Maintained regulatory, ICH-GCP, and protocol compliance, providing actionable recommendations for site performance.
• Conducted on-site and remote monitoring activities per monitoring plans and country regulations
• Followed up escalated adverse event monitoring report queries for resolution.
• Verified informed consent processes for subject confidentiality, safety and clinical data integrity.
• Confirmed documentation for site staff changes, assessing training compliance with updated requirements.
• Submitted performance feedback to stakeholders, keeping project teams on track.
• Defined project scope, milestones and task allocation to establish and maintain clear progress plans.

Overseeing the operations of the COVID-19 clinical trial, with over 20,000 enrolled subjects.

• Responded promptly to site issues with optimum solutions to prevent delays.
• Conducted regular site inspections to comply with safety guidelines.
• Kept workforce in compliance with operational standards and safety regulations by closely monitoring activities.
• Managed and led a [100]+ staff team to achieve and exceed KPI targets continuously.
• Handled negotiations with outside vendors and service agencies.
• Streamlined processes to improve and optimize office operations.
• Analysed and resolved complex resource management issues.

Worked with a leading professor at the pharmaceutical faculty and contributed mainly to completing one of the leading research projects.

• Contributed to department and faculty meetings to continuously assess and improve internal practices.
• Facilitated workshops, tutorials, and seminars, providing opportunities to stimulate students' critical thinking and analysis.

• Planned, coordinated, and executed research projects.
• Modernized syllabus, updating with current research, new techniques, and latest findings to improve relevancy.
• Coordinated laboratory experiments.
• Presented at industry-leading conferences and seminars to share research.