Francisca Chika Diala

Topic: Blood-py: Revolutionizing blood cell classification through Deep Learning Analyzing blood classification and developing different models. Deep learning solution for automated detection and classification of peripheral blood cells. Utilizes CNN, particularly U-Net for segmention and pre-trained models for feature extraction. Enhances accuracy and efficiency in haematological diagnostics, addressing challenges of manual inspection

Ensure accurate eTMF maintenance and archiving. Support start-up study procedures and documentation submissions. Assist Clinical Trial Teams and CRAs, manage contracts, change orders, and resource requests. Maintain key trial info in CTMS, manage project operations, and coordinate site-related documents. Prepare and distribute study documentation. File and upload documents accurately. Act as a liaison, provide training, and improve processes for compliance and efficiency in clinical trials.

eTMF, EDL application, reviewing cases with investigators, Study documents and to ensure the inspection condition. Represent in Studies teams. Represent the clinical documentation, Contribution to departmental development through training and mentoring, as well as data management, audit and inspections, clinical trials overview, GCP - documents and Registration Authorities.

Image processing in cell tracking force, Image modeling with matlab and imagej: Topic parcticle Tracking strategy to determine cellular traction force. ( Full Time Internship)

Analyzing blood classification and developing different models. Deep learning solution for automated detection and classification of peripheral blood cells. Utilizes CNN, particularly U-Net for segmention and pre-trained models for feature extraction. Enhances accuracy and efficiency in haematological diagnostics, addressing challenges of manual inspection

Topic: Epidemiology of Cancer and Prevention Strategies

Arzneimittel-Entwicklung, Pharmazie und Pharmakologie, Gesetzliche Grundlagen und Regularien, Essentielle Dokumente und Datenmanagement, Monitoring Visits und Reports, Einreichungen und Behörden, Qualitätsicherung und Kontrolle, Arzneimittelsicherheit, medizinische Produkte

Ethical Issues in Human subject Research; Roles and Responsibilities of the Investigator; Roles and Responsibilities of the Institution; Regulatory Issues e.g. FDA Guidance regarding Clinical Trials, ICH Guideline for Good Clinical Investigators and Mass Media.