Joyce Oladepo
Brookhaven,GA
Summary
Dynamic Clinical Research Associate with a proven track record at Takeda Pharmaceuticals, excelling in site management and pharmacovigilance. Expert in electronic data capture and detailed documentation, I enhance project outcomes through effective collaboration and quality assurance, consistently improving processes and ensuring compliance with regulatory standards.
Overview
2026
2026
years of professional experience
1
1
Certification
Work History
Clinical Research Associate/Pharmacovigilance Associate
Virtual Vocations
01.2024 - 05.2025
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
- Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
- Conducted clinical trial in accordance with protocol and recorded and monitored progress.
Quality Control/Assurance Associate
Takeda Pharmaceuticals
02.2021 - 12.2022
- Assisted with independent internal and external audits.
- Supported audit preparation through research, analysis and presentation development.
- Responsible for providing quality on the shop floor support for IG/ Albumin purification,and fill/finish operations.
- Identify and access regulatory and quality risk in activities and processes according to regulatory agency rules, guidelines and the company quality practices.
- Released finished products after reviewing samples for [Type].
- Developed corrective action plans to improve overall quality of IG/Albumin purification
Medical Laboratory Scientist
Institute Of Human Virology, Ihvn
2013 - 02.2015
- Performed pre-analytical, analytical and post-analytical processing procedures.
- Documented test results using manual transcription methods.
- Maintained high levels of laboratory safety by adhering to strict guidelines and conducting regular safety audits streamlined to H.I.V patients
- Consistently met or exceeded performance targets related to accuracy, efficiency, productivity, and customer satisfaction metrics within the lab setting.
- Increased patient satisfaction through timely and accurate diagnostic results.
Education
Bachelor of Science - Microbiology
Obafemi Awolowo University
Ile-Ife, Nigeria12-2012
Skills
- Site management
- Pharmacovigilance
- Detailed documentation
- Electronic data capture
Certification
- Introduction to Drug Safety and Pharmacovigilance Training -
- Safety Reporting in Clinical Trials[ Adverse Event Reporting]
- Clinical Trial Safety Reporting Requirements in EU and USA
- Drug Safety; Signal detection and management in Pharmacovigilance
- Drug Safety; Risk Management Planning for Medicinal Products
- Drug Safety; Urgent Safety Restrictions
- Drug Safety; Good Pharmacoepidemiology Practice
Timeline
Clinical Research Associate/Pharmacovigilance Associate
Virtual Vocations
01.2024 - 05.2025
Quality Control/Assurance Associate
Takeda Pharmaceuticals
02.2021 - 12.2022
Medical Laboratory Scientist
Institute Of Human Virology, Ihvn
2013 - 02.2015
Bachelor of Science - Microbiology
Obafemi Awolowo University