TAIWO OLUWAFUNMILOLA ABIFARIN

662-***-**** ad2tzv@r.postjobfree.com

Highly motivated Clinical Research Professional with vast knowledge in Good Clinical Practice (GCP) and ICH standards, FDA regulations and Data Management; well committed to ensuring the integrity, quality, and compliance of clinical trials while promoting patient safety WORK EXPERIENCE

Research Assistant, Mississippi State University- August 2020- Present

Conduct laboratory experiments, including techniques such as protein purification, DNA/RNA analysis, chromatography, and spectroscopy.

Perform PCR and Agarose gel Electrophoresis

Collected and recorded experimental data meticulously.

Performed data analysis using relevant software tools.

Followed safety protocols and ensured a clean and organized work environment.

Contribute to the writing of research papers, reports, and presentations.

Present research findings at lab meetings, conferences, or seminars. Clinical Research Coordinator, National Institute of Pharmaceutical Research and Development, Nigeria - February 2018- March 2019

Monitored subject enrollment, eligibility criteria, and informed consent procedures to ensure patient safety and compliance with all applicable regulatory requirements, such as Good Clinical Practice (GCP) guidelines and institutional policies.

Assisted in the development and review of study-related documents, such as protocols, informed consent forms, and clinical study reports.

Assisted in preparing regulatory submissions and reporting adverse events as required. Maintained and organized study documentation, including study binders, source documents, and electronic records

Assisted in the participant recruitment and screening activities, ensuring compliance with inclusion/exclusion criteria and ethical guidelines EDUCATION

PhD Biochemistry – May 2024

Mississippi State University

Master of Science in Botany- May 2019

University of Fort Hare, South Africa

Bachelor of Science in Biochemistry- October 2014 University of Ilorin, Nigeria

CORE SKILLS

Good Clinical Practice (GCP) standards, Data Management, Clinical Trial Management System, Electronic Data Capture (EDC), Microsoft Excel, Research Protocols, Communication and Teamwork

CERTIFICATIONS AND TRAININGS

Responsible Conduct of Research (ID- 53615749)

Good Clinical Practice – Social and Behavioral Research Best Practices for Clinical Research (ID-56645852)

Good Clinical Practice- NIDA Clinical Trials Network

Data Management for Clinical Research

Clinical Trials Data Management and Quality Assurance- John Hopkins University

Responsible Conduct of Research. ID- 53615749

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