Niyi Daisi
Edmonton,Alberta
Summary
Experienced clinical research professional with expertise in conducting clinical research in compliance with regulations, including GCP and company SOPs. Demonstrates a strong commitment to privacy and safety standards and effectively coordinates with internal departments for successful study coordination. Skilled in protocol evaluation, study documentation, screening, subject admission, inpatient care, outpatient visits, monitoring visits and study closure.
Overview
16
16
years of professional experience
1
1
Certification
Work History
Clinical Research Patient Recruiter
Phamaron
Baltimore, MD
02.2021 - 06.2023
- Collaborated with the study team to identify potential patient populations that meet the
study criteria and target enrollment numbers. - Utilized various recruitment strategies and channels to identify and engage potential study
participants, including but not limited to community outreach, online advertising, physician
referrals, patient databases, and social media platforms. - Screened potential participants to assess their eligibility for specific clinical trials based on predetermined inclusion and exclusion criteria.
- Explained the purpose, procedures, risks, and benefits of the clinical trial to potential participants, ensuring their understanding of the study and obtaining informed consent.
- Established and maintained effective relationships with healthcare providers, community organizations, patient advocacy groups, and other relevant stakeholders to facilitate patient recruitment efforts.
- Adhere to all applicable regulatory guidelines, company Standard Operating Procedures (SOPs), and ethical standards to ensure the protection of patient rights, privacy, and confidentiality.
Clinical Research Coordinator
Victoria Hospital
Prince Albert, SK
07.2021 - 01.2023
- Kept patient care protocols and clinical trial operations in compliance.
- Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
- Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
- Monitored subject enrollment and tracked dropout details.
- Conducted screening interviews to determine eligibility of possible subjects.
- Maintained accurate and complete records of study activities in accordance with regulatory requirements
- Conducted monitoring visits to ensure study compliance and data quality
- Prepared study reports and assisted with manuscript development and submission
- Maintained current knowledge of regulatory requirements and industry best practices
Clinical Research Associate
SGS||Obafemi Awolowo University Teaching Hospital Complex, Ile
Ile-Ife, NG
02.2015 - 11.2020
- Assisted in the coordination and execution of clinical trials• Conducted patient screenings and maintained study documentation
- Ensured that all study-related procedures were performed in accordance with protocol and GCP guidelines
- Conducted clinical research in compliance with regulations and company SOPs
- Evaluated protocols and informed consent forms prior to ethics committee submission
- Created and maintained study documentation consistent with the approved protocol
- Coordinated with lab staff to ensure timely receipt of screening results
- Managed study supplies and inventory and worked closely with site personnel to ensure study compliance and data quality
- Assisted with data entry and data management tasks
- Prepared and maintained study-related files and records
- Participated in sponsor and regulatory agency audits
- Coordinated movement of laboratory samples by establishing and enforcing security and safety standards
- Communicated with vendors to deliver appropriate clinical supplies to key areas and meet ongoing operational demands.
Clinical Dentist
Obafemi Awolowo University Teaching Hospital Complex, Ile
Ile-Ife, NG
02.2007 - 01.2015
- Analyzed X-rays and reviewed patients' health backgrounds to devise appropriate treatment course.
- Explained procedures, answered questions and administered additional pain relief to help patients feel comfortable.
- Conducted oral cancer screenings by thoroughly examining patients' mouths to identify problematic areas.
- Treated infections caused by chronic and acute issues and diseases within soft oral tissues.
Education
Bachelor of Science - Environmental Public Health
Concordia University of Edmonton
Edmonton, AB04.2024
Ph.D. - Biomedical Physiology
Obafemi Awolowo University
Ile-Ife01.2023
Bachelor of Dentistry - Dentistry
Obafemi Awolowo University
Ile-Ife NG02.2007
Skills
- Medical Terminology
- Data Management
- Problem Resolution
- Good Clinical Practice (GCP) and regulatory compliance
- Site initiation and Monitoring
- Protocol evaluation and IRB submission
- Study documentation and source document creation
- Proficient knowledge of Microsoft Office
- Subject screening and enrollment management
- Inpatient and outpatient study coordination
- Collaboration with internal department
- Study closure and archiving
- Excellent communication and empathy
- Good team player
- Risk Assessment and Management
Certification
- Clinical Research Associate, Viares College - 2022
- Association for Project Management (APM) PMP
- ICH-GCP, NIDA - 2022
- Pharma Drug Regulatory Affairs Certificate Course - DRA 2023
Timeline
Clinical Research Coordinator
Victoria Hospital
07.2021 - 01.2023
Clinical Research Patient Recruiter
Phamaron
02.2021 - 06.2023
Clinical Research Associate
SGS||Obafemi Awolowo University Teaching Hospital Complex, Ile
02.2015 - 11.2020
Clinical Dentist
Obafemi Awolowo University Teaching Hospital Complex, Ile
02.2007 - 01.2015
Bachelor of Science - Environmental Public Health
Concordia University of Edmonton
Ph.D. - Biomedical Physiology
Obafemi Awolowo University
Bachelor of Dentistry - Dentistry
Obafemi Awolowo University
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