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Adeola Lawal

@adeolalawal1

Clinical research coordinator pursuing study operations at Alimentiv, with healthcare scheduling and biotechnology research partnership experience.

Canada
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What I'm looking for

I’m interested in applying my coordination and documentation skills to clinical trial project coordination and study operations at Alimentiv.

At CBI Health, I coordinated healthcare scheduling and service delivery involving staff, clinicians, patients, and families across Alberta. I managed schedules and service changes while handling confidential healthcare information.

At Nimble Science, I supported research partnership development in gastrointestinal and microbiome research. I researched prospective collaborators, maintained stakeholder records, and helped coordinate scientific engagement activities.

My clinical research training includes the Clinical Research Coordinator Program, ICH Good Clinical Practice, Health Canada Division 5, and TCPS 2: CORE. I’m interested in applying my coordination and documentation experience to clinical trial project coordination and study operations at Alimentiv.

Experience

Work history, roles, and key accomplishments

AG

Business Development Associate

AgriAssure

Jan 2026 - Aug 2026 (7 months)

Coordinated stakeholder outreach, administrative activities, and follow-up processes within a regulatory and compliance-focused organization. Maintained CRM records, prepared reports, and tracked operational activities.

NS

Business Development Associate

Nimble Science

May 2024 - Aug 2024 (3 months)

Supported research partnership development at a biotechnology company specializing in gastrointestinal and microbiome research. Conducted scientific research and maintained over 300 stakeholder records.

Education

Degrees, certifications, and relevant coursework

CP

CITI Program

Health Canada Division 5 Training, Clinical Research

Health Canada Division 5 Training covering Canadian clinical trial regulatory requirements and responsibilities.

AC

ACRCC

Clinical Research Coordinator Program, Clinical Research

Clinical Research Coordinator Program training covering clinical trial conduct, informed consent, participant protection, source documentation, protocol adherence, research ethics, study coordination, regulatory requirements, and clinical trial budgeting.

CE

Course on Research Ethics

TCPS 2: CORE, Research Ethics

TCPS 2: CORE training in ethical research involving human participants, informed consent, confidentiality, and participant protection.

CP

CITI Program

ICH Good Clinical Practice E6(R3), Clinical Research

ICH Good Clinical Practice E6(R3) training covering clinical trial quality standards, participant safety, investigator responsibilities, and protocol compliance.

University of Calgary logoUC

University of Calgary

Master of Management, Management

Master of Management degree from the University of Calgary in 2024.

University of Calgary logoUC

University of Calgary

Bachelor of Science, Biological Sciences

Bachelor of Science in Biological Sciences from the University of Calgary in 2022.

Tech stack

Software and tools used professionally

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