Meet Shaheer
Science, systems
and the people behind them.
From biochemistry and biotechnology research to clinical operations and product ownership. Explore the experience behind the work.
About me & my careerShaheer Shafiq / Product Owner
From complex workflows to working products.
Product Owner and Product Manager
I build software for regulated environments. My work spans five products: EDC, CTMS, IWRS, eTMF and a complete CTU management system.
5
Clinical software products
EDC, CTMS, IWRS, eTMF and CTU management
25+
International trial sites
3
Published research papers
Drug delivery and diagnostic imaging
2026
Innovation Champion Award
Science, systems
Articles & ideas
Notes from building
clinical software.
Clinical systems exist to make every record traceable. Blinded review requires the opposite. Most teams solve that by moving the data. There is a better answer.
Across my career
Where I have worked and studied.
Work
Selected case studies
Product decisions, delivery and the clinical workflows behind them.
01 / Product Owner
Imaging Grading: a workflow for blinded review
A quality review gate and tokenised grading workspace bring blinded image review into the clinical data workflow.
- Blinded review
- Clinical imaging
- Regulated product
02 / Product Owner, leading a team of 12
MetDRA: eight modules, one platform, built from a blank page
Pakistan had no indigenous clinical trials platform. I owned the product that became one, and decided what got built in what order.
- Platform strategy
- Team leadership
- Regulated SaaS
03 / Product Owner
The EDC: putting study build in the hands of people who are not engineers
A form builder, an edit check library, a monitoring workflow and a database lock. The product decision was who gets to use them.
- Form builder
- Workflow design
- Compliance
- Self-service tooling
04 / Product Owner
From spreadsheets to a CTMS: the adoption problem, not the feature problem
Replacing spreadsheets is easy to build and hard to make people actually do. Launched publicly at the Clinical Trials Summit of Pakistan 2026.
- Migration
- Adoption
- Stakeholder management
- Launch
05 / Product Owner
IWRS: randomisation, dispensing and the problem of things you cannot undo
Allocation, pharmacy dispensing, drug accountability and administration records. Designing for actions that cannot be reversed.
- Randomisation
- Trial supply
- Irreversibility
- Safety critical
06 / Product Owner
The unglamorous half: documents, subjects, budget and people
Four modules nobody demos. Without them the platform is a data system, not a system a research organisation can run on.
- Scope discipline
- Document management
- Internal tooling
- Prioritisation
07 / Product Owner
CTMS: from delivery to a public launch
Clinical trial management delivery and a live demonstration at the Clinical Trials Summit of Pakistan 2026.
- Clinical trials
- Product delivery
- CTSP 2026
Standards behind the work
Clinical knowledge. Practical application.
Training and working knowledge applied to clinical data and regulated software.
ICH GCPE6(R3)
Good Clinical Practice
GCP training, protocol-led data management and site workflows.
HIPAAPRIVACY
Health information privacy
Privacy training, access controls and protection of clinical information.
21 CFRPART 11
Electronic records and signatures
Audit trails, controlled access and validation of clinical system workflows.
CDISCDATA STANDARDS
Clinical research data standards
Explore the standards that support consistent, structured clinical research data.
Inside the platform
The product, in focus.
Real interfaces with demonstration data. Select a screen for a closer look.
Independent review starts here.
Configure grading workflows and assign independent readers.
Every review, in one queue.
Track image grading requests and completion status.
Reader decisions, side by side.
Compare independent assessments in a clear results view.
The study at a glance.
Sites, queries and study progress in one operational view.
A clearer view of every site.
Organise study sites, investigators and site identifiers.
From protocol to working form.
Configure fields, branching logic and structured inputs.
Keep every query in view.
Follow data queries through resolution.
Reporting with a clear owner.
A reporting workspace with visible responsibility and access.
Allocation begins with structure.
Configure the parameters behind study randomisation.
Every action leaves a record.
Follow who changed a record, what happened and when.
Let’s talk