Ahmed Idris

About Ahmed Idris

Clinical Research Professional with over 5 years of hands-on experience in healthcare, specializing in expert clinical research coordination. Skilled in managing remote studies with an unwavering commitment to Good Clinical Practice (GCP) and FDA regulations. My track record spans IVD, Oncology, Vaccine Development, and Cardiovascular Health domains, showcasing my ability to coordinate studies, manage data, and oversee collaborative projects.Some examples of my results include: Coordinated Complex Studies with Adherence to Protocols: Successfully supporting coordination of 2 clinical research studies at Javara Inc, meticulously following SOPs, GCPs, study protocols, and regulatory requirements, ensuring the highest standards of execution and compliance. Enhanced Data Quality and Resolution: Supervised the EDC System for 5+ studies at ThreeWire Inc, promptly resolving over data queries, resulting in an impressive data quality enhancement of over 90%, contributing to the accuracy of research outcomes. Efficiency Boost through Innovation:Helped initiate clinical trial excellence revolution at Javara Inc, innovating processes, procedures, tools, and training methods that led to operational efficiency boost, reflecting your commitment to continuous improvement. Strategic Impact during the Pandemic: Provided crucial remote site assistance during the COVID-19 pandemic at ThreeWire Inc, relieving overwhelmed study teams, mitigating staffing shortages, and ensuring studies continued smoothly even amidst challenging circumstances. Streamlined Study Processes: Developed study trackers and. efficiency-focused tools for data entry and query resolution at ThreeWire Inc, achieving a 40% reduction in query resolution time and streamlining the research process for improved productivity.Elevated Participant Engagement and Satisfaction: Directed interactions with 20+ patients at the Epidemiology Clinical Research Center, achieving a remarkable 95% participant compliance rate, fostering participant rapport, and contributing to higher sponsor satisfaction.As a passionate Clinical Research Professional, I\'m excited about opportunities to leverage my skills in a new role. Let\'s connect and explore potential collaborations. Reach me at i•••••••@umn.edu.

Experience

1. Clinical Trial Associate

   Beckman Coulter Diagnostics

   Sep 2024 — Present

   Coordinated study activities, including eTMF auditing, filing Trial Master files, and maintaining consistent and accurate file structures to ensure compliance with regulatory standards. Managed specimen collection, handling, and processing, ensuring adherence to strict laboratory protocols for diagnostics. Oversaw shipping and receiving of on-site deliveries, maintaining consistent accuracy and efficiency in logistical operations. Collaborated with cross-functional teams to support study milestones and maintain project timelines. Leveraged a strong background in laboratory sciences and diagnostics to contribute to clinical research operations, ensuring high standards of quality and precision.

Education

• Mishkah University

  Bachelor's degree, Islamic Studies

• University of Minnesota

  Bachelor's degree in, Physiology, Minor: Public Health

  2014 — 2018

Skills

• Microsoft Excel
• Powerpoint
• Research
• Strategic Planning
• Microsoft Word
• Event Planning
• Cardiopulmonary Resuscitation (Cpr)
• Community Outreach
• Public Speaking
• Customer Service
• Healthcare
• Management
• Cpr Certified
• Microsoft Office
• Teamwork
• Project Management