Rita Ikhalo
@ritaikhalo
Regulatory Affairs and clinical research professional focused on compliant submissions and pharmacovigilance.
What I'm looking for
I’m a regulatory and clinical research professional and recent graduate of a Postgraduate Diploma in Clinical Research, Pharmacovigilance, and Regulatory Affairs. I’ve supported IRB submissions, amendments, and continuing reviews via Advarra, and prepared, reviewed, and maintained regulatory documents such as protocols, ICFs, and safety reports.
I ensure regulatory compliance through document version control and TMF accuracy, while collaborating with investigators and cross-functional teams to support study operations. With a pharmacy and public health background and prior regulatory/clinical pharmacist experience supporting NAFDAC compliance, inspections, and ADR documentation, I’m ready to contribute to submission-ready, ICH-GCP-aligned work.
Experience
Work history, roles, and key accomplishments
Clinical Research Assistant (Volunteer)
ClinGRO
Nov 2024 - Dec 2025 (1 year 1 month)
Assisted with clinical trial documentation, data collection, and compliance activities. Supported adherence to ICH-GCP and ethical research requirements while maintaining study logs and essential regulatory records.
Clinical Research Coordinator
Rejuvenation Dermatology Clinic
Feb 2025 - May 2025 (3 months)
Supported IRB submissions, amendments, and continuing reviews using Advarra. Prepared and maintained regulatory documents and ensured compliance with accurate TMF and document version control.
Regulatory / Clinical Pharmacist
NAFDAC
Jun 2015 - May 2016 (11 months)
Supported regulatory review and compliance activities for pharmaceutical products. Participated in pharmacovigilance (ADR documentation and safety monitoring), and helped with inspections, product evaluation, and regulatory reporting within a GMP-regulated environment.
Education
Degrees, certifications, and relevant coursework
Academy of Applied Pharmaceutical Sciences (AAPS)
Postgraduate Diploma, Clinical Research, Pharmacovigilance & Regulatory Affairs
Postgraduate Diploma in Clinical Research, Pharmacovigilance & Regulatory Affairs at Academy of Applied Pharmaceutical Sciences (AAPS) in Canada. Completed in 2025.
University
Master of Public Health, Public Health
Master of Public Health (MPH) at a University in Nigeria. Completed in 2021.
University
Bachelor of Pharmacy, Pharmacy
Bachelor of Pharmacy (B.Pharm) at a University in Nigeria. Completed in 2015.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Job categories
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