Inquiry & consultation
Understand programs that fit your profile and goals, with honest guidance on timelines and outcomes.
Why CliniWings
CliniWings is an IAO & ISO 9001:2015 certified, MSME certified, MCA registered clinical research training institute managed by ex-NIPERians and industry experts.
Our all-in-one curriculum covers CR, CDM, PV, MW, and RA with 100% practical training, case-study based learning, and AI-integrated tools for future-ready outcomes.
CR, CDM, PV, MW, and RA under one structured curriculum.
Modern AI-assisted learning to keep students industry-ready.
ATS resume, LinkedIn, soft skills, and mock interview support.
B.Pharm, M.Pharm, Pharm D, and M.Sc graduates.
Three distinct programs for B.Pharm, M.Pharm, Pharm D & life-science graduates across CR, CDM, PV, MW, and RA.
A shorter-duration, budget-friendly entry point into the clinical research industry.
A balanced option for students who want a more comprehensive diploma with modern technology.
The most comprehensive CliniWings program with highest-level certification and interview readiness.
How it works
From inquiry to placement - a clear path for your career.
Understand programs that fit your profile and goals, with honest guidance on timelines and outcomes.
Structured modules, hands-on practice, mocks, and feedback aligned with what employers expect in CR, CDM, PV, MW & RA.
CV refinement, interview coaching, and introductions so you can present your skills confidently to pharma and CRO teams.
Industry-aligned clinical research training for pharmacy and life-science graduates—GCP, trials conduct, and placement-focused practice.
Understand how interventional and observational trials are run—from protocol to database lock—with clarity on site and sponsor roles.
Clean, traceable data is the backbone of regulatory submissions—learn edit checks, reconciliation, and database lock concepts.
Case processing, narratives, and signal awareness for drug safety operations in regulated environments.
Structure, clarity, and regulatory expectations for clinical and safety documents.
Submissions, labelling hooks, and cross-market regulatory awareness for pharma products.
From registries and claims to fit-for-purpose studies supporting regulatory and access decisions.
Search strategy, screening, and synthesis methods used in evidence-based reviews.
Value demonstration for payers: outcomes, models, and real-world data integration.
A shorter-duration, budget-friendly entry point into clinical research industry roles for pharmacy and life-science graduates.
A balanced advanced diploma option with modern technology exposure and stronger mock-based preparation.
The most comprehensive advanced PG diploma-equivalent track with highest interview intensity and future-ready AI integration.
Celebrating another strong batch: Pharm D, B.Pharm, and M.Pharm graduates in CDM, PV, CR, RA, and TMF roles across leading global CROs.
Read postFrom CR and CDM to PV and RA—recent graduates show how focused clinical research training translates into offers at recognised sponsors and CROs.
Read postA dedicated pharmacovigilance cohort—B.Pharm and M.Pharm learners—secured Safety Science Analyst roles with one global safety organisation.
Read post