EZINNE ACHEBE

Maintained working knowledge of and ensured compliance with

• Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
• Maintained accurate and up-to-date case report forms and source documents for traceability.
• Developed and maintained accurate and up-to-date case report forms and source documents.
• Monitored patient safety throughout clinical trials and reported any adverse events.
• Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Gathered, processed, and shipped lab specimens.
• Followed informed consent processes and maintained records.
• Collected data and followed research protocols, operations manuals, and case report form requirements.

• Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
• Developed and maintained accurate and up-to-date case report forms and source documents.
• Monitored patient safety throughout clinical trials and reported any adverse events.
• Complied with research protocols by providing ongoing quality control audits.
• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
• Followed informed consent processes and maintained records.
• Gathered, processed, and shipped lab specimens.
• Collected data and followed research protocols, operations manuals, and case report form requirements.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.

Performed on-site facility inspection

• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Gathered, processed, and shipped lab specimens.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Collected data and followed research protocols, operations manuals, and case report form requirements.
• Developed and maintained accurate and up-to-date case report forms and source documents.
• Maintained accurate and up-to-date case report forms and source documents for traceability.
• Assisted with research protocol development.
• Educated patients regarding all facets of clinical study participation.
• Managed updates and input for patient information database.
• Demonstrated advanced knowledge of federal regulatory compliance guidelines.