Azeez Iginla
Maryland
Summary
Dedicated and detail-oriented Clinical Research Associate with extensive experience in managing and overseeing clinical trials across multiple therapeutic areas, including ophthalmology, rare diseases, cardiology, infectious diseases, neurology, and medical devices. Proficient in leading site evaluations, initiations, and closeouts. Skilled in ensuring compliance with regulatory standards while maintaining the highest levels of patient safety. Recognized for the ability to quickly master new procedures and technologies to drive efficient study execution.
Overview
6
6
years of professional experience
Work History
Clinical Research Associate
Technical Resources International Inc.
02.2022 - Current
- Lead site selection process, feasibility assessments, and site activations in accordance with study protocols
- Coordinate all phases of clinical studies from development to result analysis and interpretation
- Ensure regulatory compliance and timely resolution of site queries
- Conduct on-site visits, including site initiation, interim monitoring, and closeout visits
- Manage investigational drug accountability and reconciliation procedures
- Support site contract procedures and regulatory submissions
- Organized and presented at investigator meetings for eight protocols
Clinical Research Associate
PRA Health Sciences, Inc.
01.2019 - 01.2022
- Coordinated all phases of clinical studies and contributed to key study document preparation
- Managed four different protocols across over 18 sites in various therapeutic areas
- Conducted continuous monitoring activities (onsite and remote) and implemented site management activities to ensure compliance with protocol, GCP, and local and global regulations
- Performed source document review/verification (SDR/SDV)
- Prepared site visit reports and assisted site staff in resolving discrepancies
- Managed study timelines, identified risks, and implemented mitigations
- Liaised with study site personnel to communicate important clinical data and events
- Ensured data quality and timely reporting of adverse events
- Assisted in study start-up processes and conducted protocol training
- Maintained study compliance and readiness for audits
Education
Bachelor of Science - Business Administration
University of Lagos
08.2008
Skills
- GCP
- FDA regulations
- ICH guidelines
- Communication skills
- Interpersonal skills
- Problem-solving skills
- Microsoft Office Suite
- Electronic data capture (EDC) systems
- Independent work
- Multidisciplinary team collaboration
- Attention to detail
- Task management
Systemsproficiency
- EDC: (Medidata RAVE, IBM, Veeva Vault, C3D)
- CTMS (ORACLE CTMS)
- IRT (gxp brain, IRTClinical, Bracket)
- CRIS
- EPIC
Therapeuticareas
- Infectious Diseases
- General Medicine
- Dermatology
- Oncology
- Women's Health
- Medical Devices
- Ophthalmology
- Behavioral Health
- Cardiovascular
Timeline
Clinical Research Associate
Technical Resources International Inc.
02.2022 - Current
Clinical Research Associate
PRA Health Sciences, Inc.
01.2019 - 01.2022
Bachelor of Science - Business Administration
University of Lagos
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