Clinical research / Study delivery

From study plans to dependable evidence.

I work across clinical research, project management and data management, with quality assurance and regulatory support throughout the study lifecycle.

REDCapStataRMultilingual eCRFs
Explore my study experience ↗
Study workflow connecting planning, data collection, quality checks and documentation01PLAN02COLLECT03CHECK04DOCUMENT
Four connected disciplines, from setup to study closeout.

Study and registry experience

Across therapeutic areas and study types.

My work spans the following areas in different clinical roles. Counts are shown by category; related categories may overlap.

Diabetes
4studies
Ophthalmology
5studies
Rare diseases
2studies
Cancer
1study
Medical devices
1study
Vaccines
3studies
Nephrology registry
1registry
Multidisciplinary registry
1registry
Insulin
1study
Supplements
2studies
Infectious diseases
4studies
Cardiovascular diseases
3studies

01 / Clinical practice

Project Management

Connect study requirements, people and delivery. My experience at OIRRC, Hekma and Metrics Research spans clinical workflows, project coordination and programme priorities.

  • Study setup and delivery coordination
  • Team training and operational support
  • Clinical systems and workflow planning

02 / Clinical practice

Data Management

Build the study around reliable data. I develop REDCap studies, registries and eCRFs in multiple languages, and work with Stata and R for analysis.

  • Multilingual REDCap studies and registries
  • eCRF design, data dictionaries and cleaning
  • Data transfers, review and analysis

03 / Clinical practice

Quality Assurance

Make quality visible throughout the study lifecycle. My work includes system QC, user acceptance testing, pre-database-lock checks and participation as an auditee in computer system validation audits.

  • System QC and user acceptance testing
  • Data completeness and consistency review
  • Vendor audit and validation support

04 / Clinical practice

Regulatory

Support traceable, documented study processes. My experience connects data management plans, SOP contributions and study documentation with quality and compliance expectations.

  • Data management plans and SOP contributions
  • Protocol-aligned collection and review
  • Documented testing and audit readiness

Research foundation

Biotechnology at NUST. Clinical research in practice.

My MS in Industrial Biotechnology informs how I connect research questions, data collection and study delivery.

Explore my published research ↗
NUST, National University of Sciences and Technology