Aymen D Abukar

- Clinical Trial Associate embedded within Janssen, the pharmaceutical company of Johnson and Johnson.
- Experience working in Oncology and Neuroscience studies, SME within the Global Clinical Operations team for VIPER and ATLAS (systems used for running reports and maintaining oversight on our studies)
- Responsible for creating and maintaining project management trackers to ensure all key milestones are met, Perform quality reviews to aid each study being inspection ready at all times
- Run reports to help identify any issues that need to be dealt with for the studies, maintaining the TMF and ensure all key documentation is filed
- Assist with site and monitoring visits where needed to help with ISF review

• Facilitating and managing multiple oncology clinical trials at the Mount Vernon Cancer Centre, utilizing Inform EDC for efficient data collection and management. Responsibilities include overseeing various aspects of the trial process, including study initiation, patient recruitment, data collection, and study closeout along with being directly responsible for managing the trial master file (TMF).
  
• Collaborating closely with the research team, investigators, and sponsors to ensure strict adherence to study protocols, regulatory guidelines, and ethical standards, while also leveraging Inform EDC to streamline data entry and monitor real-time study progress.
  
• Coordinating patient recruitment efforts to ensure timely enrolment, conducting comprehensive study visits with participants, and accurately documenting all relevant data using Inform EDC to maintain data consistency and integrity throughout the trial. Additionally, responsible for organizing and submitting necessary regulatory documents for study approvals and ongoing compliance through the platform.

• Provided comprehensive clinical research support to investigators, including reviewing study documents, collecting, and maintaining study data, and ensuring regulatory compliance, and following SOPs and GCP guidelines
• Recorded and reported study findings, developing a comprehensive study database, ensuring accurate and timely data collection, reporting adverse effects and severe adverse effects, and became familiar with using the ECRF Medidata
• Assisted the investigator in meeting research study objectives within budget and regulatory requirements, preparing for and attending study monitoring visits and audits, and effectively interacting with patients during visits

• Learned laboratory maintenance, including waste disposal, equipment calibration, and safe handling of hazardous materials
• Gained experience in data analysis and interpretation, including statistical analysis, record keeping and communication of findings
• Acquired skills in laboratory techniques commonly used in in vivo research, such as electrophoresis, centrifugation, microscopy, and spectroscopy, and troubleshooting during experimental procedures.

• Key facilitator in maintenance and management of properties, maintaining accurate records and conducting inspections.
• Serve as a liaison between tenants and property managers to ensure smooth and efficient handover of properties and resolve discrepancies.
• Possess attention to detail, organizational skills, and effective communication abilities to fullfill responsibilities and make a positive impact in the property industry.

• Experienced Administrative Clerk at Menzies Distribution, providing operational and management support.
• Strong skills in data management, communication, organization, time management, and office procedures.
• Gained understanding of company operations and the important role of administrative support, confident in efficiently prioritizing tasks and providing exceptional support.