Isaac Ola

Skills

Clinical Data Management, Clinical Trials, Phase III Clinical Trials, Oncology, Lung Cancer, Hepatocellular Carcinoma, Rave EDC, Electronic Data Capture, EDC, eCRF, Clinical Data Validation, Data Cleaning, Data Reconciliation, Query Management, Database Freeze, Database Lock, Data Quality, Clinical Data Review, Clinical Trial Documentation, Trial Master File, TMF, Good Clinical Practice, GCP, CDISC, CDASH, SDTM, Clinical Research, Clinical Research Operations, Medical Writing, Scientific Writing, Medical Communications, Medical Editing, Manuscript Editing, Literature Reviews, Evidence Synthesis, Research Proposals, Research Reporting, Publication Support, Clinical Study Documentation, Standard Operating Procedures, SOP Development, Microsoft Excel, SPSS, STATA, EPI INFO, SQL, Power BI, Tableau, Data Visualisation, Statistical Analysis, Clinical Metrics Reporting, Research Methods, Oncology Research, Cross-Functional Collaboration, Clinical Staff Training.

About

I am a Clinical Data Manager and Medical Writer with six years of experience supporting clinical research, Phase III oncology trials, data quality, medical writing, and evidence-based research communication. I work with CROs, biotech, pharmaceutical, healthcare, and medical-communications teams that need accurate clinical-data support and clear scientific content.
My experience includes a multinational Phase III oncology study across 12 clinical sites in three countries. I support eCRF review and completion guidance, Rave EDC workflows, data validation, query generation and resolution, data reconciliation, data-quality metrics, database-freeze and database-lock activities, Trial Master File documentation, and GCP-aligned clinical-research processes. I maintained a 98% data-quality score during study execution, developed eCRF completion guidance that reduced data-entry errors by 35%, and resolved more than 200 clinical queries.
Alongside clinical data operations, I provide medical and scientific writing, literature reviews, manuscript editing, evidence synthesis, research proposals, clinical-trial documentation, research reporting, and interpretation of statistical results. I have contributed to peer-reviewed research publications and trained more than 40 clinical research professionals in data-management systems and research workflows.
My technical skills include Rave EDC, eCRF workflows, CDISC principles, CDASH, SDTM awareness, GCP, Microsoft Excel, SPSS, STATA, EPI INFO, SQL, Power BI, Tableau, data cleaning, data validation, and clinical research documentation. I am available for remote freelance, contract, and project-based clinical data-management, medical-writing, and research-support engagements.