Joao Cardeano

Biomedical Data Scientist · Analytical Chemistry & Pharmacology · AI, Bioinformatics & Health Data

Alberta, Canada

Experience

Triclinium Clinical Development

Clinical Trial Associate

Mar 2017 — Oct 2017 · 7 mos · Centurion, South Africa

–Worked within a clinical research environment providing operational, administrative, and data management support to Clinical Research Associates (CRAs) and project managers across clinical trial activities.
–Responsibilities included clinical documentation review, data handling, protocol compliance, and training in clinical trial operations under ICH-GCP guidelines.
–Tracked, investigated, and resolved over 60 Trial Master File (TMF) and protocol compliance issues, improving audit readiness and supporting sponsor confidence in trial documentation quality.
–Achieved 99% accuracy in serious adverse event (SAE) eCRF data capture and documentation, representing the highest performance metric within the company.
–Supported clinical trial operations in accordance with SOPs, ICH-GCP principles, and regulatory requirements to ensure compliance, data integrity, and participant safety.
–Reviewed and quality-checked more than 100 SAE forms for documentation errors, inconsistencies, and protocol deviations, collaborating with project managers to implement corrective actions and improve reporting accuracy.
–Participated in on-site clinical training involving data collection, source data verification, protocol adherence, and compliance monitoring within active clinical trial settings.
–Gained practical exposure to clinical trial operations including site visits, participant data handling, monitoring activities, and validation of clinical research documentation.
–Completed ICH-GCP training with emphasis on ethical conduct, regulatory compliance, participant safety, and quality standards in clinical research.

LOCKED · 11 May 2026, 21:21

University of Pretoria, Pharmacology Department

Research Scientist

Jan 2014 — Dec 2016 · 2 yr 11 mos · Pretoria, South Africa

–Worked within a multidisciplinary biomedical and analytical chemistry research environment supporting regulated clinical and translational research programmes.
–Responsibilities included method development and validation, data quality assurance, technical reporting, experimental optimisation, scientific mentorship, and interpretation of complex scientific datasets.
–Developed and optimised analytical methodologies through systematic refinement of chromatographic and mass spectrometric conditions, resulting in more than a 100% improvement in performance compared to the reference method and subsequent global adoption by the sponsor for clinical trial applications.
–Mentored and supervised four students simultaneously in analytical chemistry methodologies, experimental design, and data interpretation, contributing to the successful completion of one undergraduate, two MSc, and one PhD degree.
–Supported wildlife conservation and veterinary pharmacology research focused on the pharmacokinetics of rhinoceros immobilisation agents used in anti-poaching interventions, contributing to analytical methodologies and interpretation of biologically relevant data with potential forensic applications.

LOCKED · 11 May 2026, 21:14

Skills

ChromatographyHPLC-MS/MSMachine LearningMass SpectrometryPythonPyTorchRSQLTensorflow

Education

University of Birmingham

Master of Science · Bioinformatics · GPA: 3.8

2025

LOCKED · 11 May 2026, 19:30

University of Pretoria

Master of Science · Pharmacology · GPA: 3.7

2016

LOCKED · 11 May 2026, 20:10

University of Pretoria

Bachelor of Science Honours · Pharmacology · GPA: 3.9

2012

LOCKED · 11 May 2026, 20:24

University of Pretoria

Bachelor of Science · Medical Science · GPA: 3.4

2011

LOCKED · 11 May 2026, 20:33

Patents & publications

No patents or publications added yet.

UniTalent Verified

This candidate's record is append-only and has not been edited since submission.

Record ID: UT-2026-314667