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.
This program is designed as a shorter-duration, budget-friendly entry point into the clinical research industry.
This program is described as a balanced option for students who want a more comprehensive diploma that incorporates modern technology.
This is the most comprehensive program offered by CliniWings, providing the highest level of certification and interview preparation.
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 focused on trial lifecycle, GCP, and site-level execution readiness.
Comprehensive understanding of how clinical trials are designed, operated, and quality-controlled from protocol to close-out.
Practical CDM training for data cleaning, query management, reconciliation, and database lock readiness.
Drug safety operations training covering case intake, processing, narrative writing, and regulatory reporting basics.
Medical writing training focused on structure, clarity, consistency, and regulatory communication standards.
Regulatory Affairs training on submission pathways, labeling basics, and regulatory documentation standards.
Our learners are getting placed across top CROs, pharma, and healthcare organizations with structured interview support.
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